- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04404413
High-Intensity Interval Training and Intermittent Fasting on Body Composition and Physical Performance in Active Women
May 21, 2020 updated by: Prof. Dr. Alejandro Martínez-Rodríguez, University of Alicante
Effect of High-Intensity Interval Training and Intermittent Fasting on Body Composition and Physical Performance in Active Women
The objective of this study is to compare the body composition and physical performance effects of HIIT, with or without intermittent fasting intervention in active women.
Fourteen active normal weight women aged 18-35 participated in the study.
The effects of 2x8 weeks without (HIIT) or with (HIIT+IF) intermittent fasting caloric restriction (20% reduction in weekly energy intake) on body composition and performance (Hand-grip strength, Counter movement jump, Wingate Anaerobic 30 s Cycling Test), were compared.
There were two weeks in between both phases when they did not perform the scheduled activity, so as not to alter the experimental phase.
Study Overview
Status
Completed
Study Type
Interventional
Enrollment (Actual)
14
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Alicante
-
San Vicente Del Raspeig, Alicante, Spain, 03690
- Alejandro Martínez Rodríguez
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 35 years (ADULT)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- No muscular, ligamentous, bone, nerve or joint pathology incompatible with the training program.
- Not to present cardiovascular or cardiorespiratory problems.
- Physically active in the last 5 years, according to the American College of Sports Medicine (ACSM) definition.
Exclusion Criteria:
- Following pharmacological treatment or supplement.
- Performing other sports activities that may influence the study results during their participation in the study.
- Not following training or diet program guidelines or attending scheduled training sessions.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: HEALTH_SERVICES_RESEARCH
- Allocation: NA
- Interventional Model: SINGLE_GROUP
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
EXPERIMENTAL: PARTICIPANTS
A single-group crossover design was used to compare the effects of 2x8 weeks of high-intensity interval training without (HIIT) or with (HIIT+IF) intermittent fasting caloric restriction (20% reduction in weekly energy intake) on body composition and performance.
There were two weeks in the middle of both phases in which they did not carry out programmed activity, in order not to alter the experimental phase.
|
2x8 weeks of high-intensity interval training (HIIT)
2x8 high-intensity interval training with (HIIT+IF) intermittent fasting caloric restriction (20% reduction in weekly energy intake).
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Hand-grip strength
Time Frame: 16 weeks
|
Hand-grip strength test was performed as an indicator of overall strength.
|
16 weeks
|
Counter movement jump (CMJ)
Time Frame: 16 weeks
|
In the CMJ test, the participants performed a maximum vertical jump starting from a standing position with arm swing not allowed.
|
16 weeks
|
Wingate Anaerobic 30 s Cycling Test
Time Frame: 16 weeks
|
Wingate Anaerobic 30 s Cycling Test with a validated cycloergometer (Monark 894E, Vansbro, Sweden).
|
16 weeks
|
Fat mass
Time Frame: 16 weeks
|
Body composition masses were estimated using validated equations.
Carter's equation was used to estimate fat mass.
|
16 weeks
|
Muscle mass
Time Frame: 16 weeks
|
Body composition masses were estimated using validated equations.
Lee's equation to estimate muscle mass.
|
16 weeks
|
Residual mass
Time Frame: 16 weeks
|
Body composition masses were estimated using validated equations.
Residual mass was obtained from the difference between fat mass and muscle mass.
|
16 weeks
|
Body Mass
Time Frame: 16 weeks
|
It was performed using a digital scale with 0,1kg accuracy (Tanita BC-545, Tokyo, Japan).
|
16 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ACTUAL)
September 1, 2019
Primary Completion (ACTUAL)
September 11, 2019
Study Completion (ACTUAL)
March 1, 2020
Study Registration Dates
First Submitted
May 19, 2020
First Submitted That Met QC Criteria
May 21, 2020
First Posted (ACTUAL)
May 27, 2020
Study Record Updates
Last Update Posted (ACTUAL)
May 27, 2020
Last Update Submitted That Met QC Criteria
May 21, 2020
Last Verified
May 1, 2020
More Information
Terms related to this study
Other Study ID Numbers
- CE061811
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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