- ICH GCP
- Register voor klinische proeven in de VS.
- Klinische proef 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.
Studie Overzicht
Toestand
Conditie
Interventie / Behandeling
Gedetailleerde beschrijving
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 .
Studietype
Inschrijving (Werkelijk)
Fase
- Niet toepasbaar
Contacten en locaties
Studie Locaties
-
-
-
Cairo, Egypte
- faculty of ohysical therapy Cairo University
-
-
Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
Accepteert gezonde vrijwilligers
Geslachten die in aanmerking komen voor studie
Beschrijving
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
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: Gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Dubbele
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
|
Sham-vergelijker: 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 |
|
Experimenteel: 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 |
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Pulmonary function by (SP - electronic hand held spirometer)
Tijdsspanne: 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
Tijdsspanne: At base line and 12 weeks
|
trunk anterior flexor test |
At base line and 12 weeks
|
|
FEV 1
Tijdsspanne: at base line and 12 weeks
|
forced expiratory volume in 1 second (FEV1) [Time Frame: 12 weeks] |
at base line and 12 weeks
|
|
PEF
Tijdsspanne: at base line and 12 weeks
|
Peak expiratory flow (PEF) [Time Frame: 12 weeks] |
at base line and 12 weeks
|
|
Posterior
Tijdsspanne: at base line and 12 weeks
|
trunk posterior extensor test |
at base line and 12 weeks
|
|
right lateral
Tijdsspanne: at base line and 12 weeks
|
the right lateral plank |
at base line and 12 weeks
|
|
left rateral
Tijdsspanne: at base line and 12 weeks
|
the right lateral plank |
at base line and 12 weeks
|
Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Resting metabolic rate
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: ate base line and 12 weeks
|
Weight measurement in kilogram |
ate base line and 12 weeks
|
|
Height measurement
Tijdsspanne: at base line and 12 weeks
|
Height measurement in centimeter |
at base line and 12 weeks
|
Medewerkers en onderzoekers
Sponsor
Medewerkers
Publicaties en nuttige links
Nuttige links
Studie record data
Bestudeer belangrijke data
Studie start (Werkelijk)
Primaire voltooiing (Werkelijk)
Studie voltooiing (Werkelijk)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Werkelijk)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Andere studie-ID-nummers
- P.T.REC/012/005533
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
Beschrijving IPD-plan
not be shared
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .