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Change of Body Composition and Functional Status Following Short-term Pre-habilitation Among Morbidly Obese Patients Before Bariatric Surgery

Change of Body Composition and Functional Status Following Short-term Pre-habilitation Among Morbidly Obese Patients Before Bariatric Surgery

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04889378
Enrollment
54
Registered
2021-05-17
Start date
2021-04-15
Completion date
2022-03-14
Last updated
2022-11-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Short Term Pre-habilitation Before Bariatric Surgery

Keywords

obesity

Brief summary

Observational study is conducted in patient under short term pre-habilitation before bariatric surgery.

Detailed description

Observational study is conducted in patient under short term pre-habilitation before bariatric surgery. Data on anthropometry (waist circumference), body compositions (weight, muscle mass, fat free mass, fat mass, fat percentage and basal metabolic rate (BMR)), and functional status (handgrips strength) are collected.

Interventions

OTHERprehabilitation

very low calories diet (800-1000kcal/day) with moderate intensive aerobic exercise (1 hour per section; 3 sections per day)

Sponsors

National Cancer Institute, Malaysia
CollaboratorOTHER_GOV
Universiti Putra Malaysia
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* Obese or severe obese patients * Candidates for short term pre-habilitation among morbid obese patients before bariatric surgery * Aged more than 18 years old * Malaysian * Provided and signed informed consent

Exclusion criteria

* Not a candidate for short term pre-habilitation among morbid obese patients before bariatric surgery * Aged \<18 years old * Non-Malaysian * Not able to provide informed consent * chronic renal failure

Design outcomes

Primary

MeasureTime frameDescription
anthropometry (waist circumference in cm)baseline and after 2 weekschange in waist circumference at 2 weeks
body composition (weight in kg)baseline and after 2 weekschange in weight at 2 weeks. It will be measured by using BIA TANITA
body composition (muscle mass in kg)baseline and after 2 weekschange in muscle mass at 2 weeks. It will be measured by using BIA TANITA
body composition (fat free mass in kg)baseline and after 2 weekschange in fat free mass at 2 weeks. It will be measured by using BIA TANITA
body composition (fat mass in kg)baseline and after 2 weekschange in fat mass at 2 weeks. It will be measured by using BIA TANITA
body composition (fat percentage in percentage)baseline and after 2 weekschange in fat percentage at 2 weeks. It will be measured by using BIA TANITA
functional status (hand-grips strength in kg)baseline and after 2 weekschange in hand-grips strength at 2 weeks. Hand-grip strength will be measured by using Jammar Dynamometer

Countries

Malaysia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026