Esta página se tradujo automáticamente y no se garantiza la precisión de la traducción. por favor refiérase a versión inglesa para un texto fuente.

EFFECTS OF REFORMER PILATES TRAINING

3 de noviembre de 2026 actualizado por: Yağmur YILDIZ, Aksaray University

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.

Descripción general del estudio

Estado

Terminado

Descripción detallada

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 estudio

Intervencionista

Inscripción (Actual)

24

Fase

  • No aplica

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

18 años a 35 años (Adulto)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Femenino

Descripción

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.

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Poner en pantalla
  • Asignación: N / A
  • Modelo Intervencionista: Asignación de un solo grupo
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
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.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Pittsburgh Sleep Quality Index (PSQI)
Periodo de tiempo: 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 resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Depression-Anxiety-Stress Scale (Short Form)
Periodo de tiempo: 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

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

Publicaciones y enlaces útiles

La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el estudio.

Publicaciones Generales

  • 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

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

15 de marzo de 2026

Finalización primaria (Actual)

15 de agosto de 2026

Finalización del estudio (Actual)

30 de agosto de 2026

Fechas de registro del estudio

Enviado por primera vez

14 de septiembre de 2026

Primero enviado que cumplió con los criterios de control de calidad

2 de noviembre de 2026

Publicado por primera vez (Actual)

3 de noviembre de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

5 de noviembre de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

3 de noviembre de 2026

Última verificación

1 de noviembre de 2026

Más información

Términos relacionados con este estudio

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Descripción del plan 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.

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

Suscribir