NCT07411248

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

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Monitor

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Jan 2025

Geographic Reach
1 country

1 active site

Status
recruiting

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

Completed
12 months until next milestone

First Submitted

Initial submission to the registry

December 19, 2025

Completed
2 months until next milestone

First Posted

Study publicly available on registry

February 13, 2026

Completed
17 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 2, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 2, 2026

Completed
Last Updated

February 13, 2026

Status Verified

January 1, 2026

Enrollment Period

1.2 years

First QC Date

December 19, 2025

Last Update Submit

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

EXPERIMENTAL
Other: Face-to-Face Supervised Exercise

Mobile App-Based Exercise

EXPERIMENTAL
Device: Mobile App-Based Exercise

Home-Based Video Exercise

EXPERIMENTAL
Other: Home-Based Video Exercise

Interventions

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.

Face-to-Face Supervised Exercise

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.

Mobile App-Based Exercise

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.

Home-Based Video Exercise

Eligibility Criteria

Age18 Years - 35 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

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)

RECRUITING

MeSH Terms

Conditions

Sedentary Behavior

Condition Hierarchy (Ancestors)

Behavior

Central Study Contacts

Begüm Kara Kaya, Asst. Prof.

CONTACT

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

Locations