- ICH GCP
- Registro de ensaios clínicos dos EUA
- Ensaio Clínico NCT07911917
EFFECTS OF REFORMER PILATES TRAINING
The Effects of Reformer Pilates Training on Sleep Quality and Mental and Physical Health Outcomes in Sedentary Women: A Randomized Controlled Trial
This study investigated the effects of a 5-week Reformer Pilates exercise program on sleep quality, depression, anxiety, stress, and body mass index in 26 sedentary women. Participants completed 10 exercise sessions, with two sessions per week. Sleep quality and mental health were assessed before and after the intervention using the Pittsburgh Sleep Quality Index and Depression Anxiety Stress Scales-21. Following the program, significant improvements were observed in sleep quality, depression, stress, and body mass index. These findings suggest that Reformer Pilates may be a beneficial exercise approach for improving selected physical and psychological outcomes in sedentary women.
Visão geral do estudo
Status
Condições
Intervenção / Tratamento
Descrição detalhada
Purpose: Pilates is a widely utilized exercise therapy modality aimed at improving physical fitness, body composition, and both physical and psychological well-being in healthy populations. The aim of this study was to comprehensively investigate the effects of a Reformer Pilates (RP) exercise program on levels of depression, anxiety, and stress, as well as on sleep quality and body mass index.
Methods: Twenty-six sedentary women participated in this study. Participants completed a RP exercise program consisting of 10 sessions over a 5-week period, with two sessions per week. Sleep quality and mental health status were evaluated using the Pittsburgh Sleep Quality Index (PSQI) and the Depression Anxiety Stress Scales-21 (DASS-21), respectively. Body mass index (BMI) was calculated from participants' height and body mass measurements. All outcome measures were assessed before the exercise program and immediately following its completion.
Keywords: Reformer pilates, sleep quality, depression, anxiety, stress, body mass index.
Tipo de estudo
Inscrição (Real)
Estágio
- Não aplicável
Contactos e Locais
Locais de estudo
-
-
Aksaray
-
Aksaray, Aksaray, Turquia (Türkiye), 68100
- Aksaray University
-
-
Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
Aceita Voluntários Saudáveis
Gêneros Elegíveis para o Estudo
Descrição
Inclusion Criteria:
- Women aged 18-35 years.
- Having a sedentary lifestyle.
- Not having participated regularly in a Reformer Pilates exercise program previously.
- Voluntarily agreeing to participate in the study.
- Providing written informed consent.
- Agreeing to participate in all study assessments and the 5-week Reformer -Pilates exercise program.
Exclusion Criteria:
- Failure to attend the Reformer Pilates exercise sessions regularly.
- Failure to complete the 10-session exercise program.
- Participation in another regular exercise program during the study period.
- Having a musculoskeletal injury or health condition that prevents participation in exercise.
- Failure to complete any of the study assessments.
- Voluntary withdrawal from the study during the study period.
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Triagem
- Alocação: N / D
- Modelo Intervencional: Atribuição de grupo único
- Mascaramento: Nenhum (rótulo aberto)
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
|
Experimental: RP GRUP
Twenty-six sedentary women participated in this study . Participants completed a RP exercise program consisting of 10 sessions over a 5-week period, with two sessions per week. Sleep quality and mental health status were evaluated using the Pittsburgh Sleep Quality Index (PSQI) and the Depression Anxiety Stress Scales-21 (DASS-21), respectively. Body mass index (BMI) was calculated from participants' height and body mass measurements. All outcome measures were assessed before the exercise program and immediately following its completion. |
As part of the study, participants took part in a RP exercise programme scheduled for two days a week and comprising a total of 10 sessions. The exercise programme was structured in accordance with the principle of controlled progression, taking into account the participants' sedentary lifestyles. The sessions were conducted under the supervision of a qualified instructor with expertise in RP (SM); throughout the exercises, emphasis was placed on correct posture, breath control and movement integrity. Care was taken to ensure that all participants were subjected to the same exercise content and conditions throughout the programme. The exercise sessions were planned to include warm-up, the main exercise programme and cool-down phases. The exercise programme was implemented systematically, taking into account the principles of weekly periodisation. |
O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Pittsburgh Sleep Quality Index (PSQI)
Prazo: Baseline and immediately after the 5-week intervention
|
Measure: Pittsburgh Sleep Quality Index (PSQI) total score Scale name: Pittsburgh Sleep Quality Index (PSQI). Minimum score: 0. Maximum score: 21. Interpretation: Higher scores indicate poorer sleep quality, whereas lower scores indicate better sleep quality. |
Baseline and immediately after the 5-week intervention
|
Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Depression-Anxiety-Stress Scale (Short Form)
Prazo: Baseline and immediately after the 5-week intervention
|
Measure: Depression Anxiety Stress Scales-21 (DASS-21) scores for depression, anxiety, and stress Scale name: Depression Anxiety Stress Scales-21 (DASS-21). Minimum score: 0 for each subscale. Maximum score: 21 for each subscale. Subscales: Depression, anxiety, and stress (7 items each). Interpretation: Higher scores indicate higher levels of depression, anxiety, and stress, respectively. |
Baseline and immediately after the 5-week intervention
|
Colaboradores e Investigadores
Patrocinador
Publicações e links úteis
Publicações Gerais
- Adıgüzel, S., Aras, D., Gülü, M., Aldhahi, M. I., Alqahtani, A. S., & Al-Mhanna, S. B. (2023). Comparative effectiveness of 10-week equipment-based pilates and diaphragmatic breathing exercise on heart rate variability and pulmonary function in young adult healthy women with normal BMI-a quasi-experimental study. BMC Sports Science, Medicine and Rehabilitation, 15(1), 82. Ağargün, M. Y. (1996). Validity and reliability of Turkish version of Pittsburgh sleep quality index. Türk Psikiyatri Dergisi, 7, 107. Aibar-Almazán, A., Hita-Contreras, F., Cruz-Díaz, D., de la Torre-Cruz, M., Jiménez-García, J. D., & Martínez-Amat, A. (2019). Effects of Pilates training on sleep quality, anxiety, depression and fatigue in postmenopausal women: A randomized controlled trial. Maturitas, 124, 62-67. A'Naja, M. N., Batrakoulis, A., Camhi, S. M., McAvoy, C., Sansone, J. S., & Reed, R. (2024). 2025 ACSM worldwide fitness trends: future directions of the health and fitness industry. ACSM's Health & Fitness Journal, 28(6), 11-25. Ashrafinia, F., Mohammadizadeh, S., & Fathizadeh, N. (2014). The effects of Pilates exercise on sleep quality in postpartum women. Journal of Bodywork and Movement Therapies, 18(2), 190-199. https://doi.org/10.1016/j.jbmt.2013.09.007 Buysse, D. J., Reynolds III, C. F., Monk, T. H., Berman, S. R., & Kupfer, D. J. (1989). The Pittsburgh Sleep Quality Index: a new instrument for psychiatric practice and research. Psychiatry research, 28(2), 193-213. Caldwell, K., Harrison, M., Adams, M., & Triplett, N. T. (2009). Effect of Pilates and taiji quan training on self-efficacy, sleep quality, mood, and physical performance of college students. Journal of bodywork and movement therapies, 13(2), 155-163. Caldwell, K., Harrison, M., Adams, M., & Triplett, N. T. (2009). Effect of Pilates and Taiji Quan training on self-efficacy, sleep quality, mood, and physical performance of college students. Journal of Bodywork and Movement Therapies, 13(2), 155-163. https://doi.org/10.1
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo (Real)
Conclusão Primária (Real)
Conclusão do estudo (Real)
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Real)
Atualizações de registro de estudo
Última Atualização Postada (Real)
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Mais Informações
Termos relacionados a este estudo
Palavras-chave
Termos MeSH relevantes adicionais
Outros números de identificação do estudo
- 2025/42
Plano para dados de participantes individuais (IPD)
Planeja compartilhar dados de participantes individuais (IPD)?
Descrição do plano IPD
Individual participant-level data will not be shared publicly because the dataset contains potentially identifiable participant information. To protect participant privacy and confidentiality, individual-level data will not be made publicly available. Aggregate study results will be reported in accordance with applicable ethical and data protection requirements.
Informações sobre medicamentos e dispositivos, documentos de estudo
Estuda um medicamento regulamentado pela FDA dos EUA
Estuda um produto de dispositivo regulamentado pela FDA dos EUA
Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .