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Effect of Exercise on GDF-15 Levels in Prediabetic Patients

S

Sultan Abdulhamid Han Training and Research Hospital, Istanbul, Turkey

Status

Enrolling

Conditions

PreDiabetes

Treatments

Behavioral: Exercise

Study type

Interventional

Funder types

Other

Identifiers

NCT04799938
ACTİVE GD-15

Details and patient eligibility

About

The aim of this study is to evaluate whether there is a change in GDF-15 levels in individuals with prediabetes at the 2nd hour after the first exercise and after a 12-week exercise program with guide-based exercise programs.

Full description

GDF-15, which has anorexigenic effects, increases with exercise. In prediabetic patients, GDF-15 is higher than healthy controls. The effect of exercise on GDF-15 levels in prediabetic patients is unknown.

The aim of this study is to evaluate whether there is a change in GDF-15 levels after the application of guideline-based exercise programs in individuals with prediabetes at the 2nd hour after the first exercise and after a 12-week exercise program.

Enrollment

70 estimated patients

Sex

Female

Ages

30 to 50 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Body mass index 30-34.9 kg / m2
  • Sedentary life-style (Physical activity below 300 kcal / day will be assessed by Minnesota Leisure Physical Activity Questionnaire)
  • Those who have sufficient motivation to participate in the exercise program (will be evaluated by face-to-face interview by the researchers)
  • Having the same weight for 6 months before participating in the study (± 2.5 kg)
  • Those diagnosed with prediabetes by oral glucose tolerance test and / or HbA1c measurement will be included.

Exclusion criteria

  • Serious medical condition (e.g. advanced malignancy or major neurological, psychiatric or endocrine disease, respiratory failure, etc.)
  • Having cardiovascular disease
  • Having diabetes
  • Using metformin
  • Taking hormone replacement therapy
  • less than 1 year life expectancy
  • HIV positivity
  • Substance use
  • Functional dependence
  • Cognitive weakness
  • Those with other diseases that will affect the study result (respiratory diseases, muscle diseases, etc.)
  • Those who use drugs or supplements that will affect the results of the study

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

70 participants in 3 patient groups

İntevention group
Active Comparator group
Description:
Prediabetic patients with age 30-50 and overweight Standart recommendations Exercise intervention will be made.
Treatment:
Behavioral: Exercise
Control group
No Intervention group
Description:
Prediabetic patients with age 30-50 and overweight Only Standart recommendations
Metformin Group
No Intervention group
Description:
Prediabetic patients who received metformin Standart recommendations

Trial contacts and locations

1

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Central trial contact

Elif Yıldırım Ayaz, M.D.

Data sourced from clinicaltrials.gov

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