NCT05777265

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
29

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Mar 2023

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

March 8, 2023

Completed
7 days until next milestone

Study Start

First participant enrolled

March 15, 2023

Completed
6 days until next milestone

First Posted

Study publicly available on registry

March 21, 2023

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 15, 2023

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 15, 2023

Completed
Last Updated

August 4, 2023

Status Verified

August 1, 2023

Enrollment Period

4 months

First QC Date

March 8, 2023

Last Update Submit

August 3, 2023

Conditions

Keywords

HealthExercisePhysical FitnessWomen

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

EXPERIMENTAL

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

Other: Circuit Training

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.

Training Group

Eligibility Criteria

Age18 Years - 45 Years
Sexfemale(Gender-based eligibility)
Gender Eligibility Detailsbeing women
Healthy VolunteersYes
Age GroupsAdult (18-64)

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)

Location

MeSH Terms

Conditions

Motor Activity

Interventions

Circuit-Based Exercise

Condition Hierarchy (Ancestors)

Behavior

Intervention Hierarchy (Ancestors)

Physical Conditioning, HumanExerciseMotor ActivityMovementMusculoskeletal Physiological PhenomenaMusculoskeletal and Neural Physiological Phenomena

Study Officials

  • Derya Ozer Kaya

    İzmir Katip Celebi University

    PRINCIPAL INVESTIGATOR
  • Seyda Toprak Celenay

    Ankara Yildirim Beyazıt University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
SINGLE GROUP
Model Details: A prospective clinic study with 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

Locations