MedPath

Strength Training for Men Living With Obesity

Not Applicable
Completed
Conditions
Obesity
Registration Number
NCT04680455
Lead Sponsor
University of New Brunswick
Brief Summary

Emerging evidence suggests that alternative obesity management strategies need to address barriers to engaging with regular physical activity to adopt healthier lifestyles. It is hypothesized that more men living with obesity who are exposed to an online home-based circuit strength training for 12 weeks will be more physically active, 34 weeks after the intervention compared with people who are not exposed to the program.

Detailed Description

Sixty men (age ≥ 18 years; body fat % ≥ 25) were randomly assigned to the intervention group (N=30) or the control condition (N=30) for 12 weeks. The intervention group did the online delivered circuit training, three sessions in a week. Adherence to the weekly physical activity guidelines was evaluated 46 weeks after being enrolled in the program using a heart rate tracker and an exercise log. Most variables (anthropometrics, body composition, resting heart rate, blood pressure, lipids profile, glucose) were measured at baseline and after 12, 24, and 46 weeks. Aerobic fitness and comfort with technology were measured at baseline. Perceived benefits/barriers of participation in exercise were captured at baseline and 12 weeks.

More participants in the intervention group adhered to the physical activity guidelines compared to the control group at 46 weeks (intervention 36.8% vs control 5.3%; p=0.021). However, the intervention group did not improve their health outcomes after 12, 24, and 46 weeks. Fewer barriers were reported after 12-week for the intervention group (p=0.02).

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
60
Inclusion Criteria
  • men
  • Body fat% of 25% or more
  • Not reaching physical activity guidelines (150 min of moderate to vigorous intensity of aerobic exercises + two sessions of resistance training)
  • being able to do weight training
Exclusion Criteria
  • Taking medications that can cause to change in heart rate

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Physical activity Level48 weeks

Adherence to the both components of the physical activity guidelines

Secondary Outcome Measures
NameTimeMethod
Muscle mass46 weeks

Body composition

Cardiorespiratory fitnessBaseline

Maximum volume of oxygen consumption (Vo2peak)

Body fat percentage46 weeks

Body composition

Metabolic profile46 weeks

High density lipoprotein, low density lipoprotein, triglyceride, resting heart rate, blood pressure

BMI46 weeks

Anthropometrics

Waist circumference46 weeks

Anthropometrics

Trial Locations

Locations (1)

University of New Brunswick

🇨🇦

Fredericton, New Brunswick, Canada

University of New Brunswick
🇨🇦Fredericton, New Brunswick, Canada
© Copyright 2025. All Rights Reserved by MedPath