The Effects of 16-Week Circuit Training in Healthy Women
1 other identifier
interventional
29
1 country
1
Brief Summary
The aim of this study is to investigate the effects of 16-week CT on physical fitness parameters, pulmonary function, and quality of life in healthy women.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Mar 2023
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
March 8, 2023
CompletedStudy Start
First participant enrolled
March 15, 2023
CompletedFirst Posted
Study publicly available on registry
March 21, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 15, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
July 15, 2023
CompletedAugust 4, 2023
August 1, 2023
4 months
March 8, 2023
August 3, 2023
Conditions
Keywords
Outcome Measures
Primary Outcomes (4)
Body Mass Index (kg/m2)
Body Mass Index (kg/m2) will be assessed with the Bioelectrical Impedance Analysis System.
Sixteen week
Waist(cm)/Hip(cm) Ratio (%)
Waist(cm)/Hip(cm) Ratio (%) will be assessed with the Bioelectrical Impedance Analysis System.
Sixteen week
Muscle Strength
Muscle strength will be assessed with the isokinetic dynamometer Biodex System-4 Pro (Biodex, Shirley, New York), which is a valid and reliable method. The strength of right/left knee flexor, and extensor muscles of the participants will be determined by mean peak torque at '60°/sec and 180°/sec angular velocities.
Sixteen week
Flexibility
Flexibility will be assessed with the sit-and-reach test, which is a valid, and reliable method. Participants will be asked to reach forward as far as possible three times without bending their knees after one trial. The obtained values (cm) will be recorded and the best value will be used for analysis.
Sixteen week
Secondary Outcomes (5)
Forced Expiratory Volume in 1 Second (FEV1) (L/sec)
Sixteen week
Forced Vital Capasity (FVC) (L)
Sixteen week
FEV1/FVC (%)
Sixteen week
Peak Expiratory Flow (PEF) (L/min)
Sixteen week
Life Quality
sixteen week
Study Arms (1)
Training Group
EXPERIMENTALCT will be applied to the participants, taking into account the recommendations of the American College of Sports Medicine (ACSM), 3 days a week, an average of 40 minutes a day, for a total of 16 weeks
Interventions
CT will be applied to the participants, taking into account the recommendations of the American College of Sports Medicine (ACSM), 3 days a week, an average of 40 minutes a day, for a total of 16 weeks. Warm-up and cool-down protocols will be applied before and after each CT, and each exercise will be performed as 15 repetitions and an average of 40 seconds of rest will be given between exercises. Also, the intensity of CT will be determined according to the Borg scale (between 11 and 14). CT will include 'mini squat', 'step up', 'sit ups', 'reverse sit ups', 'leg press', 'leg curl', 'leg extension', 'crunches', 'lunge', 'prone bridge', and 'side bridge' exercises.
Eligibility Criteria
You may qualify if:
- volunteering to participate in study
- not have any musculoskeletal disease
You may not qualify if:
- history of malignancy
- using any drugs or supplement
- history of any surgery
- being pregnant
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
İzmir Katip Celebi University
Izmir, Turkey (Türkiye)
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Derya Ozer Kaya
İzmir Katip Celebi University
- PRINCIPAL INVESTIGATOR
Seyda Toprak Celenay
Ankara Yildirim Beyazıt University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Lecturer
Study Record Dates
First Submitted
March 8, 2023
First Posted
March 21, 2023
Study Start
March 15, 2023
Primary Completion
July 15, 2023
Study Completion
July 15, 2023
Last Updated
August 4, 2023
Record last verified: 2023-08
Data Sharing
- IPD Sharing
- Will not share
The investigators do not want to share individual participant data