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Article

Rowing Training in Breast Cancer Survivors: A Longitudinal Study of Physical Fitness

by
Juan Gavala-González
1,
Ismael Gálvez-Fernández
2,*,
Pere Mercadé-Melé
3 and
José Carlos Fernández-García
2
1
Department of Physical Education and Sports, University of Seville, 41013 Seville, Spain
2
Department of Didactics of Languages, Arts and Sport, University of Malaga, Andalucia-Tech, IBIMA, 29071 Malaga, Spain
3
Department of Statistics and Econometrics, University of Malaga, Andalucia-Tech, 29071 Malaga, Spain
*
Author to whom correspondence should be addressed.
Int. J. Environ. Res. Public Health 2020, 17(14), 4938; https://doi.org/10.3390/ijerph17144938
Submission received: 5 May 2020 / Revised: 20 June 2020 / Accepted: 6 July 2020 / Published: 9 July 2020

Abstract

:
The aim of this study was to determine whether a rowing training program leads to improvements in physical fitness and body composition in women who have survived breast cancer (53.70 ± 7.88 years). The participants (n = 30) completed a twelve-week training program consisting of three sessions per week, with each session lasting from sixty to ninety minutes. An anthropometric and general physical fitness assessment was performed before and after the program. The results showed statistically significant improvements in all the physical fitness tests performed: sit and reach (2.82 cm); back scratch, dominant (3.29 cm); back scratch, non-dominant (4.59 cm); counter movement jump (1.91 cm); hand grip, dominant (2.54 kgf); hand grip, non-dominant (2.53 kgf); chair stand (2.56 rep); and six-minute walk (51.56 m). In addition, a significant improvement was observed in the efficiency of the cardiovascular system measured by heart rate, in beats per minute (bpm), both before (−12.63 bpm) and after the six-minute walk test (−11.46 bpm). The evaluated body composition parameters also improved, specifically total lean mass (2.18 kg) and the percentage of total body fat (−2.63%). We can therefore conclude that rowing training programs can be a strategy to be considered for improving physical fitness in this population given the improvement obtained in both anthropometric and physical fitness variables, thus leading to better health and quality of life.

1. Introduction

According to the International Agency for Research on Cancer (IARC), breast cancer is the most common cancer worldwide, affecting 2.1 million individuals each year and is the leading cause of death among women. In 2018, approximately 627,000 women lost their lives to breast cancer [1].
According to the 2018 IARC study, 4% of women worldwide will have breast cancer at some time in their lives [2]. This percentage is increasing, and it is expected that in 2040, the percentage of women who will be affected by this type of cancer will double, rising to 8% of the global population [3].
In contrast, breast cancer is no longer fatal but is becoming chronic, as the rate of survivors is above 70% five years after intervention. This percentage is associated with the effectiveness of treatments, to the increase in early diagnosis and to the prevention of relapse [4,5]. However, the risk of relapse 20–30 years after diagnosis is rather high [6]. The increase in life expectancy of these individuals is evidence that more people are living with the side effects of breast cancer treatment (loss of muscle mass and strength, loss of mobility and disability of the upper extremities, lymphedema, fatigue and cardiac toxicity) [7].
Physical activity decreases the duration and intensity of fatigue [8,9], reduces anxiety and depression [10], increases muscle mass and strength, decreases disability in the upper extremities [11] and improves quality of life [12,13], as well as restoring and even improving functionality and well-being in women who have overcome breast cancer [14]. Several meta-analyses and reviews affirm that physical activity also contributes to reducing the risk of breast cancer recurrence [15,16,17,18,19,20,21,22,23,24,25,26,27,28], while others have obtained neutral results, implying that physical activity does not cause any changes [29,30,31].
Currently, the literature provides no scientific evidence on the prescription and structure of physical exercise for breast cancer survivors [17,18]. Consequently, this study followed the recommendations of the American College of Sports Medicine (ACSM), which state that cancer survivors should perform 150 min of moderate aerobic activity or 75 min of vigorous aerobic activity per week and resistance training two days per week [32]. Physical exercise plays an important role in improving quality of life [11] and preventing or delaying the onset of other diseases in cancer survivors [15,16,17,18,19,20,21,22,23,24] by improving aerobic capacity and muscle strength [11] and reducing fatigue [8], all of which are key elements in recovery from this disease and its sequelae [32].
With regard to existing studies on physical activity and breast cancer, we highlight the study by Di Blasio et al. (2017) in which they carried out a strength program resulting in improved physical fitness [33]. The study by Keilani et al. (2016) implemented an aerobic program and found improvements in quality of life and physical fitness [34]. Studies that implemented mixed programs [35,36,37] reported improvements in physical fitness and body composition. Among them is the research by Dieli-Conwright et al. (2018), in which a combined 16-week aerobic and resistance program significantly improved fitness, with increases in both upper and lower extremity strength [35]. Similarly, Thomas et al. (2018) carried out a 12-month training program, finding a decrease in body fat (0.9%; 1 kg/m2) and an increase in lean mass (0.5 kg), as well as improved upper and lower extremity strength [36]. Modalities such as yoga and pilates also provide beneficial results in joint mobility, muscle strength and quality of life [20,23,27]. Finally, several studies on the effects of dragon boat training programs on breast cancer survivors have identified improvements in joint mobility ranges [38], strength in different body segments [38,39] and quality of life [40,41,42].
In our study, rowing was prescribed as the basis for a physical exercise program. This sport was chosen because it involves the muscles of both the lower and upper extremities [43] and almost all the muscles of the body [44], although the main feature differentiating rowing from most other sports is the cyclic and alternating action of the flexion and extension of the upper and lower limbs and the stabilizing muscles of the trunk and back during paddling to enhance technique [45]. While the existing literature on physical activity and breast cancer is scarce, in the case of rowing and breast cancer it is non-existent. For this reason, we believe that our study may represent an important advance in the prescription of healthy exercise for breast cancer survivors. Several studies have been conducted on dragon boat training and breast cancer [42,46,47,48,49], although a brief biomechanical analysis reveals that this is an asymmetric sport requiring compensatory effort and a series of difficult movements that are not recommended in this population. In contrast, rowing is a comprehensive sport that develops the lower, upper, front, back, right and left sides of the body in almost identical proportions, since the movement is symmetrical. At the same time, the position of the body segments is much more advisable for women who have suffered from cancer and surgery affecting the upper limbs, since rowing does not require forced movements.
The aim of this study was to determine how a training program based on the sport of rowing may affect physical fitness and body composition in women who have survived breast cancer.

2. Materials and Methods

2.1. Design and Participants

The participants, all of whom were breast cancer survivors, and whose main characteristics are in Table 1, were recruited into a rowing club. Once selected, they met with the project coordinator, who explained the nature of the study, indicating that their anonymity would be maintained at all times, following the ethical considerations of Sport and Exercise Science Research [50] and in accordance with the principles included in the Declaration of Helsinki [51], which defines ethical guidelines for research on human subjects, and the University of Málaga gave the registered identification number for the ethics committee: 2020/REGSED-17007. All the participants signed a written informed consent form. In addition, during the entire intervention and thereafter, action was taken under the provisions of Organic Law 3/2018, of 5 December, on the Protection of Personal Data and the guarantee of digital rights regarding the protection of personal data in the Spanish legislation.

2.2. Instruments

Weight was measured to the nearest 0.1 kg using a Tanita model BC730 scale, following the protocol of the manufacturer for clothing and previous intake of liquids or food. Height was measured to the nearest 0.1 cm with a SECA model 213 portable stadiometer, according to the Frankfurt plane for body positioning. In the evaluation of body fat and muscle mass, a dual-energy X-ray densitometer (DXA, Hologic Explorer, Waltham, MA, USA) was used.
In addition, participants completed the physical fitness tests described below:
The sit and reach test [52] is used as a general test of flexibility. The subject sits on the floor with knees straight, legs extended and with the soles of the feet pressed firmly against the box. The arms are extended forward with the palms facing downwards on the upper surface of the scale. In this position, the subject reaches forward as far as possible and holds the position. The score is the most distant point reached and held on the fourth movement. The test administrator stands close beside the scale and records the most distant line touched by the fingertips of both hands. If the hands reach unevenly, the hand reaching the shorter distance determines the score. The score is recorded to the nearest half inch. If the reach appears to be exactly half-way between two lines, the score is based on the last line actually touched. The best value of two observations was considered. The scale on the sit and reach box has an accuracy of 5 mm.
The hand grip test [53] is used to measure the maximum isometric strength of the hand and forearm muscles. To start, the hand dimension is first measured, and then the grip area of the dynamometer is adjusted according to the length of the hand. Measurements were obtained under standardized conditions, with the participants in the seated position, elbow at ninety degrees and handle adjusted to the second position. After receiving an explanation of the procedures and becoming familiarized with the instrument, maximum grip strength should be applied for 3 to 5 s. The procedure was performed three times with each hand alternately, with an interval of one minute between each measurement. The highest value of three observations for each hand was considered. A TKK-5401 model digital hand dynamometer was used, which has a measuring range of 0.5 to 100 kg-force (kgf) and a minimum unit of measurement of 0.1 kgf.
The counter movement jump [54] measures explosive and elastic force. It is performed with the subject starting from an upright position and with the hands on the hips. Then, an upward jump is performed by means of flexion followed as quickly as possible by extension of the legs. Knee flexion should reach an angle of ninety degrees and the trunk should be prevented from bending in order to eliminate any positive influence on the jump other than from the lower extremities. The legs during the flight phase should be extended and the feet at the moment of contact with the platform should be supported first by the metatarsal area and then by the back of the foot. Measurements were taken with the My Jump 2 mobile application [55].
The six-minute walk test [56] is a cardio-respiratory function test that measures the maximum distance a subject can walk for six minutes on a flat surface. The heart rate per minute is taken before and after the test.
The chair stand test [57] assesses lower extremity strength by measuring the number of times the patient sits down and stands up from a chair, stabilized for safety. The subject sits in the center of the chair, with feet spread apart and resting on the floor. The arms are crossed and held close to the chest. From the sitting position, the subject stands up completely and then sits down again, repeating this cycle for 30 s. The final score is obtained by counting the total number of full squats (each time the subject stands up).
The back scratch test [58] evaluates flexibility in the upper extremities. The subject stands up and with the dominant hand must touch the shoulder of the same arm. With the fingers extended, the subject must advance along the back, bringing the elbow up until trying to reach the middle of the back. The other arm reaches around the back with the palm facing outwards, the goal being to touch the middle fingers of both hands behind the back. The distance between the tips of the middle fingers of both hands is measured. If the fingertips touch, the score is zero. If they do not touch, the score is negative, and if they overlap, the score is positive.

2.3. Procedure

Each participant, barefoot and wearing light clothing, underwent an initial anthropometric assessment of weight and height to calculate BMI. Subsequently, each participant performed the physical tests in the following order: hand grip, counter movement jump, back scratch, sit and reach, chair stand and six-minute walk.
After the initial assessment, the participants completed a program of twelve consecutive weeks of rowing training (Table 2). For this program, each week included three days of training lasting between sixty and ninety minutes per session. These sessions were supervised by a personal trainer who ensured attendance, correct execution of the tasks and the intensity of the sessions, in addition to excluding from the study those participants who did not meet at least 90% participation. The training period was divided into three stages, with each stage lasting four weeks and each week having three sessions. The intensity and technical difficulty of these stages was progressively increased and was regulated through the subjective perception of the effort of the participants, using the Börg scale [59].
At the end of the twelve-week training program, the participants were re-evaluated using the same procedure used in the initial evaluation.

2.4. Data Analysis

The data were collected in an Excel spreadsheet, including age, height, weight, BMI, the results of the different tests and participant affiliations. Statistical analyses were performed using the Statistical Package for Social Sciences, version 25 (IBM Corp., New York, NY, USA).
To examine whether there were significant differences resulting from the rowing training, we analyzed the differences between the means of each variable pre- and post-training and then conducted parametric testing with Student’s t-test for related samples (paired data). Prior to this analysis, the normality of the distribution was verified through the Shapiro–Wilk test (p-value > 0.05 in all the variables under study). Regarding women’s age, 30.43% are aged 41 to 50, 52.17% from 51 to 60 years old and 17.39% from 61 to 70 years old.

3. Results

Table 3 shows the means of the different variables both before and after training as well as their differences and comparisons to determine whether there are statistically significant differences. All the participants showed improvements in all the variables studied. In addition, these differences were all statistically significant except in the variables weight, BMI and total body fat, which although they improved after training, were not statistically significant: (diffWeightPost-Pre = −0.37 ± 2.58; t = −0.798; p = 0.431; diffBMIPost-Pre = −0.14 ± 1.02; t = −0.786; p = 0.438; diffTotal Body FatPost-Pre = −1.77 ± 7.6; t = −1.28; p = 0.211). The variables sit and reach (diffPost-Pre = 2.82 ± 1.87; t = 8.24; p = 0.000); back scratch, dominant (diffPost-Pre = 3.29 ± 3.15; t = 5.72; p = 0.000); back scratch, non-dominant (diffPost-Pre = 4.59 ± 3.90; t = 6.44; p = 0.000); counter movement jump (diffPost-Pre = 1.91 ± 1.71; t = 6.12; p = 0.000); hand grip, right (diffPost-Pre = 2.54 ± 1.56; t = 8.93; p = 0.000); hand grip, left (diffPost-Pre = 2.53 ± 1.91; t = 7.22; p = 0.000); chair stand (diffPost-Pre = 2.56 ± 1.71; t = 8.19; p = 0.000); heart rate at the start of the 6-min walk test (diffPost-Pre = −12.63 ± 14.68; t = −4.71; p = 0.000); heart rate at the end of the 6-min walk test (diffPost-Pre = −11.46 ± 28.39; t = −2.21; p = 0.000); distance travelled in the 6-min walk test (diffPost-Pre = 51.56 ± 48.26; t = 5.85; p = 0.000); total lean mass (diffPost-Pre = 2.18 ± 4.81; t = 2.48; p = 0.019); and percentage of total body fat (diffPost-Pre = −2.63 ± 5.43; t = −2.65; p = 0.013) all showed significantly positive differences between pre- and post-training. Practically all the variables that show statistically significant differences present the size of the effects, calculated from the Cohen’s d for a paired sample, being greater than 0.8. Therefore, the differences are statistically significant and clinically relevant.
In the following graphs, the variables can be observed grouped according to strength, aerobic, heart rate, flexibility and anthropometry. The graphs show how the variables have evolved before and after training and ratify the differences that have been analyzed in Table 2.
Figure 1 shows how all strength variables improve after training, with statistically significant differences. The chair stand test is the one with the greatest absolute difference (diffPost-Pre = 2.56 ± 1.71).
Figure 2 shows the aerobic variable, distance in the six-minute walking test, and a clear improvement is observed after training (diffPost-Pre = 51.56 ± 48.26).
Figure 3 graphically analyzes the heart rate variables and clearly shows how these two variables decrease significantly due to training.
Figure 4 graphically displays the flexibility variables where they all present better results after training, all of which are statistically significant.
Figure 5 shows the anthropometric variables where all of them improve after the training tests. These differences are statistically significant.
To sum up, the results in Table 3 are displayed graphically in the five figures. All aerobic, strength and flexibility variables improve, since they present higher values after training. Heart rate variables improve by decreasing tensions at the end of the activity. Finally, the anthropometric variables improve by lowering the value of weight, body mass index, total body fat and percentage of total body fat, in addition to increasing the total lean mass once the rowing activity is finished.

4. Discussion

The study of breast cancer from the perspective of physical activity is relatively recent, as demonstrated by the limited literature and recommendations published by the ACSM [31] less than six months ago. A previous analysis identified only a small number of articles indicating that physical activity causes neither a positive nor a negative reaction in breast cancer survivors [29,30,31]. Most studies, however, have found that physical activity in individuals with breast cancer leads to a range of improvements, the most notable being a decrease in the perception of fatigue [8,9] and the delay or absence of other diseases such as breast cancer recurrence [15,16,17,18,19,20,21,22,23,24].
Physical activity has been shown to improve quality of life in breast cancer survivors [12,13] and functionality [14] in an isolated way or associated with aspects of physical fitness, including both joint mobility and muscle strength [20,23,27]. Through activities such as yoga or pilates [20,23], aerobic activities [32], specific strength programs [33], combined aerobic and muscle strength exercises [35,36,37] or the practice of dragon boat [42,46,47,48], improvements in physical fitness have been found, especially in strength in the extremities [36,37] as well as in body composition [35].
Several studies have conducted aerobic [33] or strength programs [34], which resulted in improvements in quality of life and physical fitness. However, it should be noted that most of the previous studies implemented mixed interventions following the recommendations of the ACSM [32]. In our rowing training program, the duration was twelve weeks, and the findings identified significant improvements in both the anthropometric and physical fitness variables analyzed. These results are in line with those of Dieli-Conwright et al. (2018) and Thomas et al. (2018), in which improvements in anthropometric variables were reported after a program of sixteen weeks and twelve months, respectively [35,36].
In our study, based on the administration of a rowing training program, improvements were observed in all body composition parameters evaluated through DXA, which decreased total body fat and percentage of total body fat and increased lean mass (Table 3). All of these improvements were significant and greater than in any previous studies in the literature.
In addition, the results pertaining to physical fitness showed significant improvements in the different standardized tests that measure a wide range of manifestations of physical fitness including upper extremity and hip range of motion, lower and upper extremity strength, aerobic capacity and heart rate at rest and after prolonged effort.
Consequently, the results of our study can contribute to improving the health and quality of life of women who have overcome breast cancer, offering them a new strategy for physical exercise prescription for a problem that affects more than two million women each year.

5. Conclusions

Our research offers a novel methodological proposal for physical exercise prescription after breast cancer through a training program based on rowing, a cyclic and symmetrical sport that combines overall strength with aerobic endurance. This new proposal has a relatively short duration, twelve weeks, and is capable of bringing about improvements in all aspects of physical fitness and cardiac function during stress, as well as in anthropometric parameters such as fat and lean mass.

Author Contributions

I.G.-F. and J.G.-G. conceived and conceptualized the study. I.G.-F. and P.M.-M. collected and analyzed the data. I.G.-F., J.C.F.-G., J.G.-G. and P.M.-M. conducted the necessary literature reviews and drafted the first manuscript. J.C.F.-G. provided critical feedback and helped shape the analysis and manuscript. All authors contributed to the revision and writing of the final draft. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the “Researching in Sport Sciences” research group (CTS-563) of the Andalusian Research Plan.

Acknowledgments

We would like to thank the Real Club Mediterraneo of Malaga, its rowing captain: Juan Carlos Marfil Rodríguez and the team of the Malaga Dragon Boat BCS for opening their doors to us, giving us all the facilities in the world and for giving us the most important thing: their time and inspiring us with their impetus and energy, thanks to which we can present the first results of this study. To Maria Repice, for her help with the English version of this manuscript. Finally, we would also like to thank Alejandro Sánchez for his participation in the data collection for this study.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. World Health Organization. Breast Cancer: Prevention and Control. Available online: https://www.who.int/topics/cancer/breastcancer/en (accessed on 11 April 2020).
  2. International Agency for Research on Cancer. Cancer Today. Available online: https://gco.iarc.fr/today/home (accessed on 14 April 2020).
  3. International Agency for Research on Cancer. Cancer Tomorrow. Available online: https://gco.iarc.fr/tomorrow/home (accessed on 14 April 2020).
  4. Cantarero-Villanueva, I.; Fernández-Lao, C.; Del Moral-Avila, R.; Fernández-de-Las-Peñas, C.; Feriche-Fernández-Castanys, M.B.; Arroyo-Morales, M. Effectiveness of core stability exercises and recovery myofascial release massage on fatigue in breast cancer survivors: A randomized controlled clinical trial. Evid. Based Complement. Alternat. Med. 2012, 2012, 620619. [Google Scholar] [CrossRef] [Green Version]
  5. Anthis, N.J.; Kavanaugh-Lynch, M.H.E. The Global Challenge to Prevent Breast Cancer: Surfacing New Ideas to Accelerate Prevention Research. Int. J. Environ. Res. Public Health 2020, 17, 1394. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  6. Dixon, J.M.; Montgomery, D. Follow-up after breast cancer. BMJ 2008, 336, 107–108. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  7. Soriano-Maldonado, A.; Carrera-Ruiz, Á.; Díez-Fernández, D.M.; Esteban-Simón, A.; Maldonado-Quesada, M.; Moreno-Poza, N.; del Mar García-Martínez, M.; Alcaraz-García, C.; Vázquez-Sousa, R.; Moreno-Martos, H.; et al. Effects of a 12-week resistance and aerobic exercise program on muscular strength and quality of life in breast cancer survivors: Study protocol for the EFICAN randomized controlled trial. Medicine 2019, 98, e17625. [Google Scholar] [CrossRef] [Green Version]
  8. Romero-Barquero, C. Actividad física en el tiempo libre previene enfermedades cardiacas/cardiovasculares: Una revisión sistemática. Rev. Iberoam. Cienc. Act. Física y Deporte 2020, 9, 1–22. [Google Scholar] [CrossRef] [Green Version]
  9. Vázquez Rigueira, P.; Pedrero Chamizo, R.; Aparicio Ugarriza, R.; Santiago Dorrego, C.; Calonge, S.; Gómez, F.; Le Ble, G.P.; Manjón, R.D.; Meléndez, A.; Barrios, L.; et al. Efectos de un programa de ejercicio intradiálisis en pacientes con enfermedad renal crónica. Rev. Iberoam. Cienc. Act. Física y Deporte 2019, 8, 52–66. [Google Scholar] [CrossRef]
  10. Moros, M.T.; Ruidiaz, M.; Caballero, A.; Serrano, E.; Martínez, V.; Tres, A. Effects of an exercise training program on the quality of life of women with breast cancer on chemotherapy. Rev. Médica de Chile 2010, 138, 715–722. [Google Scholar] [CrossRef] [Green Version]
  11. Mascherini, G.; Tosi, B.; Giannelli, C.; Grifoni, E.; Degl’innocenti, S.; Galanti, G. Breast cancer: Effectiveness of a one-year unsupervised exercise program. J. Sports Med. Phys. Fit. 2019, 59, 283–289. [Google Scholar] [CrossRef]
  12. Pennington, K.P.; McTiernan, A. The role of physical activity in breast and gynecologic cancer survivorship. Gynecol. Oncol. 2018, 149, 198–204. [Google Scholar] [CrossRef]
  13. Aranda-Malavés, R.; Tudela-Desantes, A.; González-Ródenas, J. Academic and athletic performance in young athletes from the Sports Technification Centre in Cheste. Educ. Sport Health Phys. Act. 2019, 3, 86–94. [Google Scholar]
  14. Lope, V.; Martín, M.; Castelló, A.; Casla, S.; Ruiz, A.; Baena-Cañada, J.M.; Casas, A.; Calvo, L.; Bermejo, B.; Muñoz, M.; et al. Physical activity and breast cancer risk by pathological subtype. Gynecol. Oncol. 2017, 144, 577–585. [Google Scholar] [CrossRef] [PubMed]
  15. Boyne, D.J.; O’Sullivan, D.E.; Olij, B.F.; King, W.D.; Friedenreich, C.M.; Brenner, D.R. Physical Activity, Global DNA Methylation, and Breast Cancer Risk: A Systematic Literature Review and Meta-analysis. Cancer Epidemiol. Biomark. Prev. 2018, 27, 1320–1331. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  16. Schmidt, T.; van Mackelenbergh, M.; Wesch, D.; Mundhenke, C. Physical activity influences the immune system of breast cancer patients. J. Cancer Res. Ther. 2017, 13, 392–398. [Google Scholar] [CrossRef] [PubMed]
  17. Spei, M.E.; Samoli, E.; Bravi, F.; La Vecchia, C.; Bamia, C.; Benetou, V. Physical activity in breast cancer survivors: A systematic review and meta-analysis on overall and breast cancer survival. Breast 2019, 44, 144–152. [Google Scholar] [CrossRef]
  18. Lee, J. A meta-analysis of the association between physical activity and breast cancer mortality. Cancer Nurs. 2019, 42, 271–285. [Google Scholar] [CrossRef]
  19. Lahart, I.M.; Metsios, G.S.; Nevill, A.M.; Carmichael, A.R. Physical activity for women with breast cancer after adjuvant therapy. Cochrane Database Syst. Rev. 2018, 1, CD011292. [Google Scholar] [CrossRef] [Green Version]
  20. Patsou, E.D.; Alexias, G.D.; Anagnostopoulos, F.G.; Karamouzis, M.V. Effects of physical activity on depressive symptoms during breast cancer survivorship: A meta-analysis of randomised control trials. ESMO Open 2017, 2, e000271. [Google Scholar] [CrossRef] [Green Version]
  21. Singh, B.; Spence, R.R.; Steele, M.L.; Sandler, C.X.; Peake, J.M.; Hayes, S.C. A systematic review and meta-analysis of the safety, feasibility, and effect of exercise in women with stage II+ breast cancer. Arch. Phys. Med. Rehabil. 2018, 99, 2621–2636. [Google Scholar] [CrossRef] [Green Version]
  22. Hong, F.; Ye, W.; Kuo, C.H.; Zhang, Y.; Qian, Y.; Korivi, M. Exercise intervention improves clinical outcomes, but the “time of session” is crucial for better quality of life in breast cancer survivors: A systematic review and meta-analysis. Cancers 2019, 11, 706. [Google Scholar] [CrossRef] [Green Version]
  23. Panchik, D.; Masco, S.; Zinnikas, P.; Hillriegel, B.; Lauder, T.; Suttmann, E.; Chinchilli, V.; Mc Beth, M.; Hermann, W. Effect of exercise on breast cancer-related lymphedema: What the lymphatic surgeon needs to know. J. Reconstr. Microsurg. 2019, 35, 37–45. [Google Scholar] [CrossRef]
  24. Quintana López, V.A.; Díaz López, K.J.; Caire Juvera, G. Interventions to improve healthy lifestyles and their effects on psychological variables among breast cancer survivors: A systematic review. Nutr. Hosp. 2018, 35, 979–992. [Google Scholar] [CrossRef] [PubMed]
  25. Soares Falcetta, F.; de Araújo Vianna Trésel, H.; de Almeida, F.K.; Rangel Ribeiro Falcetta, M.; Falavigna, M.; Dornelles Rosa, D. Effects of physical exercise after treatment of early breast cancer: Systematic review and meta-analysis. Breast Cancer Res. Treat. 2018, 170, 455–476. [Google Scholar] [CrossRef] [PubMed]
  26. Hardefeldt, P.J.; Penninkilampi, R.; Edirimanne, S.; Eslick, G.D. Physical activity and weight loss reduce the risk of breast cancer: A meta-analysis of 139 prospective and retrospective studies. Clin. Breast Cancer 2018, 18, e601–e612. [Google Scholar] [CrossRef] [PubMed]
  27. Pinto-Carral, A.; Molina, A.J.; de Pedro, Á.; Ayón, C. Pilates for women with breast cancer: A systematic review and meta-analysis. Complement. Ther. Med. 2018, 41, 130–140. [Google Scholar] [CrossRef]
  28. Chen, X.; Wang, Q.; Zhang, Y.; Xie, Q.; Tan, X. Physical activity and risk of breast cancer: A meta-analysis of 38 cohort studies in 45 study reports. Value Heal. 2019, 22, 104–128. [Google Scholar] [CrossRef] [Green Version]
  29. Grimley, C.E.; Kato, P.M.; Grunfeld, E.A. Health and health belief factors associated with screening and help-seeking behaviours for breast cancer: A systematic review and meta-analysis of the european evidence. Br. J. Heal. Psychol. 2020, 25, 107–128. [Google Scholar] [CrossRef]
  30. Abdin, S.; Lavallée, J.F.; Faulkner, J.; Husted, M. A systematic review of the effectiveness of physical activity interventions in adults with breast cancer by physical activity type and mode of participation. Psycho-Oncology 2019, 28, 1381–1393. [Google Scholar] [CrossRef]
  31. Chan, D.S.M.; Abar, L.; Cariolou, M.; Nanu, N.; Greenwood, D.C.; Bandera, E.V.; McTiernan, A.; Norat, T. World Cancer Research Fund International: Continuous update project—Systematic literature review and meta-analysis of observational cohort studies on physical activity, sedentary behavior, adiposity, and weight change and breast cancer risk. Cancer Causes Control 2019, 30, 1183–1200. [Google Scholar] [CrossRef] [Green Version]
  32. Campbell, K.L.; Winters-Stone, K.M.; Wiskemann, J.; May, A.M.; Schwartz, A.L.; Courneya, K.S.; Zucker, D.S.; Matthews, C.E.; Ligibel, J.A.; Gerber, L.H.; et al. Exercise guidelines for cancer survivors: Consensus statement from international multidisciplinary roundtable. Med. Sci. Sports Exerc. 2019, 51, 2375–2390. [Google Scholar] [CrossRef] [Green Version]
  33. Di Blasio, A.; Morano, T.; Cianchetti, E.; Gallina, S.; Bucci, I.; Di Santo, S.; Tinari, C.; Di Donato, F.; Izzicupo, P.; Di Baldassarre, A.; et al. Psychophysical health status of breast cancer survivors and effects of 12 weeks of aerobic training. Complement. Ther. Clin. Pract. 2017, 27, 19–26. [Google Scholar] [CrossRef]
  34. Keilani, M.; Hasenoehrl, T.; Neubauer, M.; Crevenna, R. Resistance exercise and secondary lymphedema in breast cancer survivors—A systematic review. Support. Care Cancer 2016, 24, 1907–1916. [Google Scholar] [CrossRef] [PubMed]
  35. Dieli-Conwright, C.M.; Courneya, K.S.; Demark-Wahnefried, W.; Sami, N.; Lee, K.; Sweeney, F.C.; Stewart, C.; A Buchanan, T.; Spicer, D.; Tripathy, D.; et al. Aerobic and resistance exercise improves physical fitness, bone health, and quality of life in overweight and obese breast cancer survivors: A randomized controlled trial. Breast Cancer Res. 2018, 20, 124. [Google Scholar] [CrossRef]
  36. Thomas, G.A.; Cartmel, B.; Harrigan, M.; Fiellin, M.; Capozza, S.; Zhou, Y.; Ercolano, E.; Gross, C.P.; Hershman, D.; Ligibel, J.; et al. The effect of exercise on body composition and bone mineral density in breast cancer survivors taking aromatase inhibitors. Obesity 2017, 25, 346–351. [Google Scholar] [CrossRef] [PubMed]
  37. Baumann, F.T.; Reike, A.; Reimer, V.; Schumann, M.; Hallek, M.; Taaffe, D.R.; Newton, R.U.; Galvao, D.A. Effects of physical exercise on breast cancer-related secondary lymphedema: A systematic review. Breast Cancer Res. Treat. 2018, 170, 1–13. [Google Scholar] [CrossRef] [PubMed]
  38. Fong, A.J.; Saxton, H.R.; Kauffeldt, K.D.; Sabiston, C.M.; Tomasone, J.R. “We’re all in the same boat together”: Exploring quality participation strategies in dragon boat teams for breast cancer survivors. Disabil. Rehabil. 2020, 3, 1–12. [Google Scholar] [CrossRef] [PubMed]
  39. Giganti, M.G.; Tresoldi, I.; Sorge, R.; Melchiorri, G.; Triossi, T.; Masuelli, L.; Lido, P.; Albonici, L.; Foti, C.; Modesti, A.; et al. Physical exercise modulates the level of serum MMP-2 and MMP-9 in patients with breast cancer. Oncol. Lett. 2016, 12, 2119–2126. [Google Scholar] [CrossRef] [Green Version]
  40. Melchiorri, G.; Viero, V.; Triossi, T.; Sorge, R.; Tancredi, V.; Cafaro, D.; Andretis, C.; Vulpialni, M.C.; Saraceni, V.M. New approach to evaluate late arm impairment and effects of dragon boat activity in breast cancer survivors. Medicine 2017, 96, e8400. [Google Scholar] [CrossRef] [Green Version]
  41. Mitchell, T.L.; Yakiwchuk, C.V.; Griffin, K.L.; Gray, R.E.; Fitch, M.I. Survivor dragon boating: A vehicle to reclaim and enhance life after treatment for breast cancer. Health Care Women Int. 2007, 28, 122–140. [Google Scholar] [CrossRef] [PubMed]
  42. McDonough, M.H.; Patterson, M.C.; Weisenbach, B.B.; Ullrich-French, S.; Sabiston, C.M. The difference is more than floating: Factors affecting breast cancer survivors´ decisions to join and maintain participation in dragon boat teams and support groups. Disabil. Rehabil. 2019, 41, 1788–1796. [Google Scholar] [CrossRef]
  43. DAS, A.; Mandal, M.; Syamal, A.K.; Majumdar, P. Monitoring changes of cardio-respiratory parameters during 2000 m rowing performance. Int. J. Exerc. Sci. 2019, 12, 483–490. [Google Scholar]
  44. Yoshiga, C.C.; Higuchi, M. Rowing performance of female and male rowers. Scand. J. Med. Sci. Sports 2003, 13, 317–321. [Google Scholar] [CrossRef] [PubMed]
  45. Aramendi, J.M. Remo olímpico y remo tradicional: Aspectos biomecánicos, fisiológicos y nutricionales. Arch. Med. Deporte 2014, 159, 51–59. [Google Scholar]
  46. Harris, S.R. “We’re all in the same boat”: A review of the benefits of dragon boat racing for women living with breast cancer. Evid. Based Complement. Altern. Med. 2012, 2012, 167651. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  47. Unruh, A.M.; Elvin, N. In the eye of the dragon: Women’s experience of breast cancer and the occupation of dragon boat racing. Can. J. Occup. Ther. 2004, 71, 138–149. [Google Scholar] [CrossRef]
  48. Sabiston, C.M.; McDonough, M.H.; Crocker, P.R. Psychosocial experiences of breast cancer survivors involved in a dragon boat program: Exploring links to positive psychological growth. J. Sport Exerc. Psychol. 2007, 29, 419–438. [Google Scholar] [CrossRef]
  49. Fernández-García, J.C.; Gálvez-Fernández, I.; Gavala-González, J. Estudio longitudinal sobre la pérdida de peso en mujeres jóvenes. J. Sport Health Res. 2019, 11 (Suppl. 1), 105–114. [Google Scholar]
  50. Harriss, D.; Macsween, A.; Atkinson, G. Standards for Ethics in Sport and Exercise Science Research: 2018 Update. Int. J. Sports Med. 2017, 38, 1126–1131. [Google Scholar] [CrossRef] [Green Version]
  51. World Medical Association Declaration of Helsinki. JAMA 2013, 310, 2191. [CrossRef] [Green Version]
  52. Lemmink, K.A.; Kemper, H.C.; de Greef, M.H.; Rispens, P.; Stevens, M. The validity of the sit-and-reach test and the modified sit-and-reach test in middle-aged to older men and women. Res. Q. Exerc. Sport 2003, 74, 331–336. [Google Scholar] [CrossRef]
  53. Jakobsen, L.H.; Rask, I.K.; Kondrup, J. Validation of handgrip strength and endurance as a measure of physical function and quality of life in healthy subjects and patients. Nutrition 2010, 26, 542–550. [Google Scholar] [CrossRef]
  54. Sayers, S.P.; Harackiewicz, D.V.; Harman, E.A.; Frykman, P.N.; Rosenstein, M.T. Cross-validation of three jump power equations. Med. Sci. Sports Exerc. 1999, 31, 572–577. [Google Scholar] [CrossRef] [PubMed]
  55. Haynes, T.; Bishop, C.; Antrobus, M.; Brazier, J. The validity and reliability of the My Jump 2 app for measuring the reactive strength index and drop jump performance. J. Sports Med. Phys. Fit. 2019, 59, 253–258. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  56. Cote, C.G.; Casanova, C.; Marín, J.M.; Lopez, M.V.; Pinto-Plata, V.; de Oca, M.M.; Dordetlly, L.J.; Nekach, H.; Celli, B.R. Validation and comparison of reference equations for the 6-min walk distance test. Eur. Respir. J. 2008, 31, 571–578. [Google Scholar] [CrossRef] [PubMed]
  57. Jones, C.J.; Rikli, R.E.; Beam, W.C. A 30-s chair-stand test as a measure of lower body strength in community-residing older adults. Res. Q. Exerc. Sport 1999, 70, 113–119. [Google Scholar] [CrossRef] [PubMed]
  58. Rikli, R.E.; Jones, C.J. Development and validation of criterion-referenced clinically relevant fitness standards for maintaining physical independence in later years. Gerontol. 2013, 53, 255–267. [Google Scholar] [CrossRef]
  59. Börg, G. Psychophysical bases of perceived exertion. Med. Sci. Sports Exerc. 1982, 14, 337–381. [Google Scholar] [CrossRef]
Figure 1. Strength variable. Pre = pretest; Post = post-test; CMJ = counter movement jump test; DH = dominant hand grip test; NDH = Non-dominant hand grip test; CH = chair stand test; rep = repetitions.
Figure 1. Strength variable. Pre = pretest; Post = post-test; CMJ = counter movement jump test; DH = dominant hand grip test; NDH = Non-dominant hand grip test; CH = chair stand test; rep = repetitions.
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Figure 2. Distance in the six-minute walking test. Pre = pretest; Post = post-test; 6mw = six-minute walking test.
Figure 2. Distance in the six-minute walking test. Pre = pretest; Post = post-test; 6mw = six-minute walking test.
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Figure 3. Heart rate in the six-minute walking test. Pre = pretest; Post = post-test; SHR = starting heart rate; FHR = final heart rate; bpm = beats per minute.
Figure 3. Heart rate in the six-minute walking test. Pre = pretest; Post = post-test; SHR = starting heart rate; FHR = final heart rate; bpm = beats per minute.
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Figure 4. Flexibility variable. Pre = pretest; Post = post-test; SR = sit and reach test; DBS = dominant back scratch test; NDBS = non-dominant back scratch test.
Figure 4. Flexibility variable. Pre = pretest; Post = post-test; SR = sit and reach test; DBS = dominant back scratch test; NDBS = non-dominant back scratch test.
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Figure 5. Anthropometry variable. Pre = pretest; Post = post-test; W = weight; BMI = body mass index; TBF = total body fat; TLM = total lean mass; TBFP = percentage of total body fat.
Figure 5. Anthropometry variable. Pre = pretest; Post = post-test; W = weight; BMI = body mass index; TBF = total body fat; TLM = total lean mass; TBFP = percentage of total body fat.
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Table 1. Characteristics of the sample about breast cancer.
Table 1. Characteristics of the sample about breast cancer.
Age (Years)Years from DiagnosisBreast (%)Stage (%)Surgery (%)
53.70 ± 7.886.57 ± 5.02Right26.09I4.35Preservation53.52
II30.43Total Mastectomy39.13
Left73.91III52.17
IV8.7Double Mastectomy4.35
Table 2. Exercise prescription design for the program.
Table 2. Exercise prescription design for the program.
StageContent
1Initial phase with mobility exercises, proprioceptive exercises and postural control exercises. Main phase with rowing training. Final phase with stretching. Börg scale 5–6.
2Initial phase with mobility exercises, proprioceptive exercises and postural control exercises. Main phase with rowing training. Final phase with stretching. Börg scale 6–7.
3Initial phase with mobility exercises, proprioceptive exercises and postural control exercises. Main phase with rowing training. Final phase with stretching. Börg scale 7–8.
Table 3. Statistical analysis of the studied variables. Mean ± standard deviation; differences, t-student test, effect size and p-value.
Table 3. Statistical analysis of the studied variables. Mean ± standard deviation; differences, t-student test, effect size and p-value.
VariablesPretestPost-testDiff Post-Pret-StudentEffect Sizep
Weight (kg)68.67 ± 10.9868.29 ± 10.79−0.37 ± 2.58−0.7980.140.431
BMI (kg/m2)26.34 ± 3.7826.19 ± 3.67−0.14 ± 1.02−0.7860.140.438
Total body fat (kg)27.62 ± 6.7925.85 ± 6.29−1.77 ± 7.60−1.280.230.211
Total lean mass (kg)40.43 ± 4.6142.61 ± 3.452.18 ± 4.812.4860.450.019 *
Percentage of total body fat (%)40.07 ± 4.8437.44 ± 4.88−2.63 ± 5.43−2.6570.480.013 *
Sit and reach test (cm)0.87 ± 6.613.69 ± 6.572.82 ± 1.878.2421.510.000 **
Dominant back scratch test (cm)−2.19 ± 8.221.10 ± 6.543.29 ± 3.155.7261.040.000 **
Non-dominant back scratch test (cm)−6.64 ± 7.47−2.05 ± 5.724.59 ± 3.906.441.180.000 **
Counter movement jump test (cm)14.67 ± 4.3016.58 ± 4.281.91 ± 1.716.1281.120.000 **
Dominant hand grip test (kgf)23.89 ± 4.5626.44 ± 5.002.54 ± 1.568.9331.630.000 **
Non-dominant hand grip test (kgf)21.73 ± 4.3724.26 ± 4.062.53 ± 1.917.2291.320.000 **
Chair stand test (rep)14.90 ± 2.4117.46 ± 2.752.56 ± 1.718.1941.500.000 **
Starting heart rate at six-minute walking test (bpm)98.43 ± 16.7285.80 ± 9.79−12.63 ± 14.68−4.7120.860.000 **
Final heart rate at six-minute walking test (bpm)143.26 ± 32.64131.80 ± 18.62−11.46 ± 28.39−2.2120.400.000 **
Distance in six-minute walking test (m)611.23 ± 87.01662.80 ± 85.8251.56 ± 48.265.8521.070.000 **
* = p < 0.05; ** = p < 0.001.

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MDPI and ACS Style

Gavala-González, J.; Gálvez-Fernández, I.; Mercadé-Melé, P.; Fernández-García, J.C. Rowing Training in Breast Cancer Survivors: A Longitudinal Study of Physical Fitness. Int. J. Environ. Res. Public Health 2020, 17, 4938. https://doi.org/10.3390/ijerph17144938

AMA Style

Gavala-González J, Gálvez-Fernández I, Mercadé-Melé P, Fernández-García JC. Rowing Training in Breast Cancer Survivors: A Longitudinal Study of Physical Fitness. International Journal of Environmental Research and Public Health. 2020; 17(14):4938. https://doi.org/10.3390/ijerph17144938

Chicago/Turabian Style

Gavala-González, Juan, Ismael Gálvez-Fernández, Pere Mercadé-Melé, and José Carlos Fernández-García. 2020. "Rowing Training in Breast Cancer Survivors: A Longitudinal Study of Physical Fitness" International Journal of Environmental Research and Public Health 17, no. 14: 4938. https://doi.org/10.3390/ijerph17144938

APA Style

Gavala-González, J., Gálvez-Fernández, I., Mercadé-Melé, P., & Fernández-García, J. C. (2020). Rowing Training in Breast Cancer Survivors: A Longitudinal Study of Physical Fitness. International Journal of Environmental Research and Public Health, 17(14), 4938. https://doi.org/10.3390/ijerph17144938

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