- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT06763718
Qigong Breathing Exercise on Bariatric Outcomes After Bariatric Surgery: a Randomized Controlled Clinical Trial
Effects of Modified Qigong Breathing Exercise on Physical and Metabolic Outcomes After Bariatric Surgery
Bariatric surgery has been reported to be the most effective treatment option for losing and maintaining body weight and improving comorbidities and mortality associated with morbid obesity. Nevertheless, even though physical activity is recommended to optimize bariatric surgery results. Very little is known, about whether engaging in an exercise program after surgery can provide additional improvement in health outcomes. While to date there are relatively few researches studied the effect of exercise in patients who have undergone bariatric surgery. This study was conducted to explore the influence of Modified Qigong Breathing Exercise on pulmonary function, endurance and fitness on post bariatric surgery patients.
Qigong as ancient Chinese traditional medicine have been documented to be effective in treating obesity. Literature showing that the desire to eat and the feeling of hunger, along with prospective food consumption in patients with obesity.
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Descripción detallada
Bariatric surgery has been reported to be the most effective treatment option for losing and maintaining body weight and improving comorbidities and mortality associated with morbid obesity. Nevertheless, even though physical activity is recommended to optimize bariatric surgery results. Very little is known, about whether engaging in an exercise program after surgery can provide additional improvement in health outcomes. While to date there are relatively few researches studied the effect of exercise in patients who have undergone bariatric surgery. This study was conducted to explore the influence of Modified Qigong Breathing Exercise on pulmonary function,endurance and fitness on post bariatric surgery patients.
Bariatric surgery has been reported to be the most effective treatment option for losing and maintaining body weight and improving comorbidities and mortality associated with morbid obesity. Nevertheless, even though physical activity is recommended to optimize bariatric surgery results. Very little is known, about whether engaging in an exercise program after surgery can provide additional improvement in health outcomes. While to date there are relatively few researches studied the effect of exercise in patients who have undergone bariatric surgery.
Qigong as ancient Chinese traditional medicine have been documented to be effective in treating obesity. Literature showing that the desire to eat and the feeling of hunger, along with prospective food consumption in patients with obesity .
Tipo de estudio
Inscripción (Actual)
Fase
- No aplica
Contactos y Ubicaciones
Ubicaciones de estudio
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-
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Cairo, Egipto
- faculty of ohysical therapy Cairo University
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- Both male and fem
- age ranged from 18-25 years old
- at least 6 months after BS
Exclusion Criteria:
- Patients with nerve root compression
- spine disorders
- spinal fracture
- previous spinal surgery
- pregnancy
- lower limb injury
- Any contraindication to the exercise therapy
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Doble
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Comparador falso: Control
No exercise will be given to the participants in the control group |
No exercise will be given to the participants in the control group |
|
Experimental: Modified Qigong Breathing Exercise
The exercise is recommended to be performed standing, or modified standing with trunk leaning forward and bilateral upper extremities support on countertop. Initial position: Stand up with feet shoulder-width apart, hands down along your body, or put palms on the abdomen. Take a deep breath, squaring shoulders, and pull in belly at the same time. Hold breath for 3 to 4 seconds, while keeping abdomen retracted with maximally contracting abdominal muscles. Exhale, so the shoulders go back to the starting position, while chest and abdominal muscles relax. Repeat this exercise 10 times. Note. If the stomach is difficult to draw in a standing position, it is possible to perform the exercise with both hands resting on support. |
The exercise is recommended to be performed standing, or modified standing with trunk leaning forward and bilateral upper extremities support on countertop. Initial position: Stand up with feet shoulder-width apart, hands down along the body, or put palms on the abdomen. Take a deep breath, squaring shoulders, and pull in belly at the same time. Hold breath for 3 to 4 seconds, while keeping abdomen retracted with maximally contracting abdominal muscles. Exhale, so the shoulders go back to the starting position, while chest and abdominal muscles relax. Repeat this exercise 10 times. Note. If the stomach is difficult to draw in a standing position, it is possible to perform the exercise with both hands resting on support. Duration: 30 minutes, 3 days/ week for 12 weeks |
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Pulmonary function by (SP - electronic hand held spirometer)
Periodo de tiempo: at base line and 12 weeks
|
Forced vital capacity (FVC) [Time Frame: 12 weeks] |
at base line and 12 weeks
|
|
Core endurance by McGill tests
Periodo de tiempo: At base line and 12 weeks
|
trunk anterior flexor test |
At base line and 12 weeks
|
|
FEV 1
Periodo de tiempo: at base line and 12 weeks
|
forced expiratory volume in 1 second (FEV1) [Time Frame: 12 weeks] |
at base line and 12 weeks
|
|
PEF
Periodo de tiempo: at base line and 12 weeks
|
Peak expiratory flow (PEF) [Time Frame: 12 weeks] |
at base line and 12 weeks
|
|
Posterior
Periodo de tiempo: at base line and 12 weeks
|
trunk posterior extensor test |
at base line and 12 weeks
|
|
right lateral
Periodo de tiempo: at base line and 12 weeks
|
the right lateral plank |
at base line and 12 weeks
|
|
left rateral
Periodo de tiempo: at base line and 12 weeks
|
the right lateral plank |
at base line and 12 weeks
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Resting metabolic rate
Periodo de tiempo: at base line and 12 weeks
|
Change in resting metabolic rate measured by indirect calorimetry at 0 and 12 weeks. |
at base line and 12 weeks
|
|
Percent fat mass
Periodo de tiempo: at base line and 12 weeks
|
Change in fat mass percentage measured by DXA at 0 and 12 weeks |
at base line and 12 weeks
|
|
Weight measurement
Periodo de tiempo: ate base line and 12 weeks
|
Weight measurement in kilogram |
ate base line and 12 weeks
|
|
Height measurement
Periodo de tiempo: at base line and 12 weeks
|
Height measurement in centimeter |
at base line and 12 weeks
|
Colaboradores e Investigadores
Patrocinador
Colaboradores
Publicaciones y enlaces útiles
Enlaces Útiles
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
Otros números de identificación del estudio
- P.T.REC/012/005533
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Descripción del plan IPD
not be shared
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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