Ejercicio, Creencias sobre el Dolor y Patrones de Actividad en el Dolor Musculoesquelético (EPAP)
Investigación de la Relación Entre los Beneficios y Barreras del Ejercicio, Creencias sobre el Dolor y Patrones de Actividad en Individuos que Experimentan Dolor Musculoesquelético
This observational study aims to investigate the relationship between exercise benefits and barriers, pain beliefs, and activity patterns in individuals experiencing musculoskeletal pain. Participants will complete questionnaires about their pain, exercise habits, and daily activity patterns. The study does not involve any interventions or treatments. The purpose is to better understand how beliefs and perceived barriers influence physical activity in people with musculoskeletal pain, which may help inform future strategies to improve exercise participation and overall well-being.
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Descripción detallada
This observational study will include individuals experiencing musculoskeletal pain. Participants will be asked to complete a series of questionnaires assessing pain intensity, exercise benefits and barriers, pain-related beliefs, and activity patterns. The study aims to explore the relationships among these factors to better understand how pain perceptions and perceived barriers affect physical activity.
No interventions, treatments, or medications will be administered as part of this study. All data will be collected confidentially, and participation is voluntary. Participants may withdraw from the study at any time without any consequences. The findings of this research may help inform future strategies to improve exercise adherence and overall quality of life in individuals with musculoskeletal pain.
Tipo de estudio
Inscripción (Actual)
Contactos y Ubicaciones
Ubicaciones de estudio
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Istanbul, Turquía (Türkiye)
- İstinye University Faculty of Health Sciences, Department of Physiotherapy and Rehabilitation
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Método de muestreo
Población de estudio
The study will include adults aged 18-65 years who have experienced musculoskeletal pain within the past 6 months. Participants must be able to read and understand Turkish and provide informed consent. Individuals with acute trauma, recent surgery, severe cardiovascular, neurological, or psychiatric conditions, cognitive impairments, or who are pregnant will be excluded.
Descripción
Inclusion Criteria:
Adults aged 18-65 years Experiencing musculoskeletal pain (must have experienced musculoskeletal pain within the past 6 months) Voluntarily agree to participate and provide signed informed consent Able to read and understand Turkish (to complete questionnaires accurately)
Exclusion Criteria Younger than 18 years or older than 65 years Acute trauma, recent surgery, or infection causing temporary musculoskeletal pain Severe cardiovascular, neurological, or psychiatric disorders unrelated to musculoskeletal pain Pregnant women (due to potential physiological changes affecting musculoskeletal pain) Cognitive or mental impairments preventing accurate completion of study questionnaires
Exclusion Criteria:
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Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Modelos observacionales: OTHER
- Perspectivas temporales: PROSPECTIVE
Cohortes e Intervenciones
Grupo / Cohorte |
Intervención / Tratamiento |
|---|---|
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Single Cohort
All participants experiencing musculoskeletal pain will complete questionnaires assessing pain intensity, exercise benefits and barriers, pain beliefs, and activity patterns. No interventions or treatments will be administered. |
Not applicable - observational study, no interventions administered |
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Pain Beliefs (PBQ)
Periodo de tiempo: Single assessment at survey completion
|
Participants' perceived benefits of and barriers to exercise will be assessed using the Exercise Benefits/Barriers Scale. |
Single assessment at survey completion
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Exercise Benefits and Barriers (EBBS)
Periodo de tiempo: Single assessment at survey completion
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Participants' perceived benefits of and barriers to exercise will be assessed using the Exercise Benefits/Barriers Scale. |
Single assessment at survey completion
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Pain-Related Activity Patterns (POAM-P)
Periodo de tiempo: Single assessment at survey completion
|
Participants' activity patterns in relation to pain and pain management strategies will be measured using the Pain-Related Activity Patterns Questionnaire . |
Single assessment at survey completion
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Demographic Data
Periodo de tiempo: Single assessment at survey completion
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Age, sex, education level, and occupation will be collected using a demographic questionnaire. |
Single assessment at survey completion
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Colaboradores e Investigadores
Patrocinador
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
Finalización primaria (Actual)
Finalización del estudio (Actual)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- EPAP 24-314
- No secondary ID (Otro identificador: Istinye University Human Research Ethics Committee)
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Descripción del plan IPD
The study will not share individual participant data to protect participants' privacy and confidentiality. Data include sensitive health information, and sharing it could risk identification of participants.
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
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