Back to resultsExercise Time in Sedentary Middle-aged Female
Primary Purpose
Weight Loss
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Exercise time
Sponsored by
About this trial
This is an interventional treatment trial for Weight Loss
Eligibility Criteria
Inclusion Criteria:
- Sedentary lifestyle
- Good Health
- Weight stability
Exclusion Criteria:
*Abnormality or history of Disease
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Group I
Group II
Arm Description
Study group I (57 participants) received the continuous training of exercise time.
Study group II (58 participants) received the interval training of exercise time.
Outcomes
Primary Outcome Measures
HDL-c
Secondary Outcome Measures
Full Information
NCT ID
NCT01851837
First Posted
May 4, 2013
Last Updated
February 17, 2017
Sponsor
P.L.Shupik National Medical Academy of Post-Graduate Education
1. Study Identification
Unique Protocol Identification Number
NCT01851837
Brief Title
Exercise Time in Sedentary Middle-aged Female
Official Title
Response Of Weight And Lipid Profile To Exercise Time In Sedentary Overweight/Obese Middle-Aged And Older Women
Study Type
Interventional
2. Study Status
Record Verification Date
May 2016
Overall Recruitment Status
Completed
Study Start Date
September 2012 (undefined)
Primary Completion Date
December 2015 (Actual)
Study Completion Date
March 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
P.L.Shupik National Medical Academy of Post-Graduate Education
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The exercise time is an important factor among the medical guides for weight loss; however, there is still little knowledge about exercise duration paths in middle-aged and older women. The present study aimed to determine the effects of the interval training on weight loss and lipid profile, and to compare its efficiency with the continuous training.
Detailed Description
Participants included sedentary women (age 45-75 years) with overweight or obesity (n= 115). They were randomly divided into two groups including continuous exercise, and interval exercise. The weight assessment parameters including change in weight and body composition, blood sample tests were performed pre- and three month post-intervention.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Weight Loss
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
115 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Group I
Arm Type
Active Comparator
Arm Description
Study group I (57 participants) received the continuous training of exercise time.
Arm Title
Group II
Arm Type
Active Comparator
Arm Description
Study group II (58 participants) received the interval training of exercise time.
Intervention Type
Other
Intervention Name(s)
Exercise time
Intervention Description
Continuous training, Interval training
Primary Outcome Measure Information:
Title
HDL-c
Time Frame
3 month
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
45 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Sedentary lifestyle
Good Health
Weight stability
Exclusion Criteria:
*Abnormality or history of Disease
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mohammadreza Rezaeipour, M.D.
Organizational Affiliation
Member of Scientific Board in Physical Education and Sport Sciences
Official's Role
Principal Investigator
12. IPD Sharing Statement
Learn more about this trial
Exercise Time in Sedentary Middle-aged Female
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