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Effects of Exercise Prediabetic Individuals

E

Eastern Mediterranean University

Status

Enrolling

Conditions

Prediabetes / Type 2 Diabetes

Treatments

Other: High Intensity Interval Training (HIIT)
Other: Moderate Intensity Continuous Training (MICT)

Study type

Interventional

Funder types

Other

Identifiers

NCT06831266
ETK00-2023-0184

Details and patient eligibility

About

The aim of this study was to determine the effects of two different exercise protocols on body composition, aerobic capacity, blood lipid profile, some biomarkers, quality of life and exercise beliefs in participants at risk of diabetes.

Full description

After being informed about the study and possible risks, all participants who gave written informed consent and met the eligibility requirements will be randomly assigned to 2 separate groups.

Enrollment

24 estimated patients

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Being between 18-60 years old
  • HbA1c value between 5.7%-6.4%
  • BMI>24,9 kg/m²
  • Being sedentary
  • Not on any diet

Exclusion criteria

  • Insulin and derivative drug use
  • Uncontrolled hypertension
  • History of heart disease
  • History of MI or stroke

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

24 participants in 2 patient groups

HIIT High Intensity Interval Training
Experimental group
Description:
High-intensity interval training (HIIT) is a type of training that involves repeated bouts of high intensity effort interspersed by recovery times.
Treatment:
Other: High Intensity Interval Training (HIIT)
MICT Moderate Intensity Continuous Training
Active Comparator group
Description:
Moderate Intensity Continuous Training (MICT) consists of performing aerobic exercise at a constant and moderate intensity for a prolonged duration.
Treatment:
Other: Moderate Intensity Continuous Training (MICT)

Trial contacts and locations

2

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Central trial contact

Yasin Yurt; Emine Ahsen Şenol

Data sourced from clinicaltrials.gov

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