- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving 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.
Studieoversikt
Status
Forhold
Intervensjon / Behandling
Detaljert beskrivelse
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
Registrering (Faktiske)
Fase
- Ikke aktuelt
Kontakter og plasseringer
Studiesteder
-
-
-
Cairo, Egypt
- faculty of ohysical therapy Cairo University
-
-
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Beskrivelse
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
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Dobbelt
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Sham-komparator: 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 |
|
Eksperimentell: 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 |
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Pulmonary function by (SP - electronic hand held spirometer)
Tidsramme: 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
Tidsramme: At base line and 12 weeks
|
trunk anterior flexor test |
At base line and 12 weeks
|
|
FEV 1
Tidsramme: at base line and 12 weeks
|
forced expiratory volume in 1 second (FEV1) [Time Frame: 12 weeks] |
at base line and 12 weeks
|
|
PEF
Tidsramme: at base line and 12 weeks
|
Peak expiratory flow (PEF) [Time Frame: 12 weeks] |
at base line and 12 weeks
|
|
Posterior
Tidsramme: at base line and 12 weeks
|
trunk posterior extensor test |
at base line and 12 weeks
|
|
right lateral
Tidsramme: at base line and 12 weeks
|
the right lateral plank |
at base line and 12 weeks
|
|
left rateral
Tidsramme: at base line and 12 weeks
|
the right lateral plank |
at base line and 12 weeks
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Resting metabolic rate
Tidsramme: 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
Tidsramme: 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
Tidsramme: ate base line and 12 weeks
|
Weight measurement in kilogram |
ate base line and 12 weeks
|
|
Height measurement
Tidsramme: at base line and 12 weeks
|
Height measurement in centimeter |
at base line and 12 weeks
|
Samarbeidspartnere og etterforskere
Sponsor
Samarbeidspartnere
Publikasjoner og nyttige lenker
Hjelpsomme linker
Studierekorddatoer
Studer hoveddatoer
Studiestart (Faktiske)
Primær fullføring (Faktiske)
Studiet fullført (Faktiske)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Andre studie-ID-numre
- P.T.REC/012/005533
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
IPD-planbeskrivelse
not be shared
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Studerer et amerikansk FDA-regulert enhetsprodukt
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .