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Effect of Bicycle Ergometer Training on Fat Tissue Amount and Metabolism

P

Pamukkale University

Status

Enrolling

Conditions

Endurance Training

Treatments

Other: endurance training with bicycle ergometer in termoneutral ambient temperature
Other: endurance training with bicycle ergometer in lightly cold ambient temperature

Study type

Interventional

Funder types

Other

Identifiers

NCT07263126
23.07.2024/13

Details and patient eligibility

About

The aim of this study is to investigate the effect of endurance training performed with a bicycle ergometer at different ambient temperatures on the amount of fat tissue and fat tissue metabolism in overweight and obese women.

Full description

This study will examine the effects of 12 weeks of endurance training on a bicycle ergometer at thermoneutral and slightly cold ambient temperatures on body composition, subcutaneous and visceral fat tissue thickness, and levels of irisin, leptin, adiponectin, apelin, IL-6 and FGF-21 in the blood of overweight and obese women.

Enrollment

36 estimated patients

Sex

Female

Ages

20 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Being female,

  • Being between 20-40 years old,
  • Having a BMI between 25 and 34.9,
  • Having a waist circumference greater than 80 cm,
  • Not having participated in any exercise program in the last 3 months ,
  • Not having experienced a change of more than 10% in body weight in the last 6 months.

Exclusion criteria

  • On a weight loss diet,

    • Having cancer, unstable heart disease, cerebrovascular disease, metabolic disease, diabetes, hypertension, psychiatric disorders, or other conditions or neurological disorders,
    • Having a musculoskeletal disorder or any disease/injury that may affect participation in exercise training,
    • Participating in regular physical activity (at least 150 minutes of moderate-intensity physical activity or 75 minutes of vigorous-intensity physical activity or an equivalent combination of both during the week),
    • Being pregnant or breastfeeding,
    • Having undergone surgery for the treatment of obesity,
    • Receiving pharmacological treatment for obesity. Participants who did not attend more than 20% of the endurance training program will be excluded from the study.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

36 participants in 3 patient groups

Case group 1
Experimental group
Description:
participants trained in termoneutral ambient temperature
Treatment:
Other: endurance training with bicycle ergometer in termoneutral ambient temperature
Case group 2
Active Comparator group
Description:
participants trained in lightly cold ambient temperature
Treatment:
Other: endurance training with bicycle ergometer in lightly cold ambient temperature
control group
No Intervention group
Description:
participants do not trained

Trial contacts and locations

1

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Central trial contact

Şule Şimşek, Ass. Prof.; Ayşe Nur Oymak Soysal, PhD

Data sourced from clinicaltrials.gov

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