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Efficacy of Various Aerobic Exercises on Abdominal Obesity in Women With Metabolic Syndrome.

P

Pamukkale University

Status

Completed

Conditions

Metabolic Syndrome

Treatments

Other: Supervised treadmill group (%50 VO2 max) (group 2)
Other: Supervised treadmill group (%70 VO2 max) (group 1)
Device: ECE PEDO pedometer group (%50 VO2 max) (group 3)

Study type

Interventional

Funder types

Other

Identifiers

NCT03445741
2015TPF037

Details and patient eligibility

About

Objective: To show metabolic and hormonal responses and effects on abdominal obesity of aerobic exercise in different intensity and duration and detraining period in women with metabolic syndrome.

Full description

Objective: To show metabolic and hormonal responses and effects on abdominal obesity of aerobic exercise in different intensity and duration and detraining period in women with metabolic syndrome.

Methods: Fifty-one women with metabolic syndrome were divided into three groups: 12 weekly sessions of high intensity supervised treadmill group, respectively, at % 70 of maximum oxygen consumption (group I, n=17), low intensity supervised treadmill group, respectively at % 50 of maximum oxygen consumption (group II, n=17) and walking at low intensity, respectively at % 50 of maximum oxygen consumption with ECEPEDO pedometer (group III, n=17). Target heart rate (HR) corresponding to values of 50-70 % VO2max were determined by the submaximal treadmill test. Group 1 and 2 were instructed walking at their target HR on a treadmill. The number of steps taken in a minute corresponding to target HR was determined by a criterion pedometer and group 3 was instructed walking in this step range recorded to ECE PEDO giving audible feedback. Participants were evaluated by weight, BMI, waist circumference (WC), blood sugar, LDL, HDL and triglyceride; viseral fat, trunk fat and waist circumference by bioelectrical impedance device (VIScan); ergospirometric VO2max at baseline, 12-week and 4-week detraining period.

Enrollment

60 estimated patients

Sex

Female

Ages

25 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • eligible participants who meet the criteria for inclusion were women with metabolic syndrome diagnosis according to National Cholesterol Education Program Adult Treatment Panel III (NCEP ATP III) criteria and were 25-65 years old.
  • Participants were well communicative, motivated and willing to participate in the study.

Exclusion criteria

  • The exclusion criteria were presence of uncontrolled hypertension, type 2 diabetes mellitus, atherosclerotic heart disease, using drugs to affect thyroid, lipids metabolism and insulin sensitization, musculoskeletal or systemic diseases contradicting the exercise, a neurological or psychiatric disease affecting cooperation and cognitive function.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

60 participants in 3 patient groups

Supervised treadmill group (%70 VO2 max)
Active Comparator group
Description:
Supervised treadmill group (%70 VO2 max) (group 1): The participants were instructed walking exercise at their target heart rate, (% 70 of maximum oxygen consumption) on a treadmill in Sports Rehabilitation Unit of Pamukkale University.
Treatment:
Other: Supervised treadmill group (%70 VO2 max) (group 1)
Supervised treadmill group (%50 VO2 max)
Experimental group
Description:
Supervised treadmill group (%50 VO2 max) (group 2): The participants were instructed walking exercise at their target heart rate, (% 50 of maximum oxygen consumption) on a treadmill in Sports Rehabilitation Unit of Pamukkale University.
Treatment:
Other: Supervised treadmill group (%50 VO2 max) (group 2)
ECE PEDO pedometer group (%50 VO2 max)
Experimental group
Description:
ECE PEDO pedometer group (%50 VO2 max) (group 3): The participants were instructed walking with ECE PEDO which the number of steps taken in a minute corresponding to target HR at % 50 of maximum oxygen consumption were provided.
Treatment:
Device: ECE PEDO pedometer group (%50 VO2 max) (group 3)

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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