Exercise Approaches and Physical Activity Level in Inactive Adults
Effects of Different Exercise Approaches on Physical Activity Level and Health Outcomes in Inactive Adults
1 other identifier
interventional
30
1 country
1
Brief Summary
This randomized, controlled, single-blind study aims to compare the effects of different exercise approaches on physical activity level and health-related outcomes in inactive adults. Thirty inactive individuals aged 18-35 years will be randomly assigned to supervised face-to-face group exercise, mobile application-based exercise, or video-based home exercise. Exercise programs will be performed three days per week for eight weeks and will include aerobic, strengthening, and flexibility exercises.
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 Jan 2025
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
Study Start
First participant enrolled
January 6, 2025
CompletedFirst Submitted
Initial submission to the registry
December 19, 2025
CompletedFirst Posted
Study publicly available on registry
February 13, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 2, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
March 2, 2026
CompletedFebruary 13, 2026
January 1, 2026
1.2 years
December 19, 2025
February 11, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Total Physical Activity Level
Physical activity will be assessed using the International Physical Activity Questionnaire-Short Form (IPAQ-SF). Total physical activity will be calculated as metabolic equivalent (MET)-minutes per week based on walking, moderate-intensity, and vigorous-intensity activities performed during the last 7 days. Higher values indicate higher levels of physical activity.
From baseline to the end of the intervention at 8 weeks
Secondary Outcomes (8)
Daily Step Count
From baseline to the end of the intervention at 8 weeks
Active Time
From baseline to the end of the intervention at 8 weeks
Energy Expenditure
From baseline to the end of the intervention at 8 weeks
Distance Covered
From baseline to the end of the intervention at 8 weeks
Aerobic Capacity
From baseline to the end of the intervention at 8 weeks
- +3 more secondary outcomes
Study Arms (3)
Face-to-Face Supervised Exercise
EXPERIMENTALMobile App-Based Exercise
EXPERIMENTALHome-Based Video Exercise
EXPERIMENTALInterventions
Participants will perform supervised face-to-face group exercise sessions three days per week for eight weeks under the guidance of a physiotherapist. Each session will include aerobic, strengthening, and flexibility exercises.
Participants will perform exercise sessions using the Nike+ Training Club mobile application three days per week for eight weeks. The program will include aerobic, strengthening, and flexibility exercises delivered through asynchronous video content.
Participants will perform video-based home exercise sessions using the "Walk at Home: Leslie" program three days per week for eight weeks. The program will include aerobic, strengthening, and flexibility exercises.
Eligibility Criteria
You may qualify if:
- Taking fewer than 5,000 steps per day and classified as physically inactive according to the International Physical Activity Questionnaire-Short Form (\<600 MET-min/week)
- Residing in Istanbul
- Willingness to participate in the study
You may not qualify if:
- Diagnosis of end-stage congestive heart failure
- Presence of malignant or unstable arrhythmia
- Lack of adequate infrastructure to participate in technology-based physical activity programs
- Presence of mental dysfunction
- Presence of acute musculoskeletal injury
- Pregnancy
- Answering "YES" to any item on the Physical Activity Readiness Questionnaire (PAR-Q)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Biruni University
Istanbul, Zeytinburnu, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
December 19, 2025
First Posted
February 13, 2026
Study Start
January 6, 2025
Primary Completion
March 2, 2026
Study Completion
March 2, 2026
Last Updated
February 13, 2026
Record last verified: 2026-01
Data Sharing
- IPD Sharing
- Will not share