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Clinical Trials/CTRI/2024/04/066415
CTRI/2024/04/066415CompletedPhase 3

Effect of Blood Flow Restriction Aerobic Training on Body Composition, Cardiorespiratory Performance and Quality of Life in Young Obese Females

Galgotias University1 site in 1 country50 target enrollmentStarted: May 7, 2024Last updated:

Trial Snapshot

Phase
Phase 3
Status
Completed
Sponsor
Enrollment
50
Locations
1
Primary Endpoint
Body Mass Index

Study Overview

Brief Summary

This study investigates the effects of Blood Flow Restriction (BFR) Aerobic Training on various parameters in young obese females. It explores changes in body composition, cardiorespiratory performance, and quality of life resulting from this novel exercise approach. Through controlled interventions, the research aims to elucidate the potential benefits of BFR training in improving health outcomes among this demographic. By analyzing data on body composition shifts, cardiovascular endurance enhancements, and subjective assessments of well-being, the study aims to provide insights into the efficacy of BFR aerobic training as a potential strategy for managing obesity-related health concerns in young females.

Study Design

Study Type
Interventional
Allocation
Randomized
Masking
Participant and Investigator Blinded

Eligibility Criteria

Ages
18.00 Year(s) to 25.00 Year(s) (—)
Sex
Female

Inclusion Criteria

  • BMI Grade I between 30-34.9 kg/m2 Prior to the commencement of the study, none of the participants had engaged in regular strength, resistance, and/or aerobic exercise.

Exclusion Criteria

  • Body mass index – more than Grade I Any recent Musculoskeletal injury of the lower limb Peripheral vascular disorders Any Metabolic disorder Bone and joint disease.
  • Anyone already undergoing aerobic & Resistance training Neuropsychological disorders Recent Myocardial infarction.

Outcomes

Primary Outcomes

Body Mass Index

Time Frame: Baseline and 12 weeks

Muscle strength and endurance by Dynamometer

Time Frame: Baseline and 12 weeks

Heart Rate, BP, Vo2 Max by PFT(FVC,FEV1 and ratio)

Time Frame: Baseline and 12 weeks

SPo2

Time Frame: Baseline and 12 weeks

Blood Glucose and lactic Acid Profile

Time Frame: Baseline and 12 weeks

Secondary Outcomes

  • WHOQOL- BRIEF(Baseline, 6 months and 12 months)

Investigators

Sponsor
Galgotias University
Sponsor Class
Research institution
Responsible Party
Principal Investigator
Principal Investigator

Sumera Khan

Galgotias University

Study Sites (1)

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