NCT07762781

Brief Summary

The aim of this study is to evaluate the effectiveness of a commercially available mobile exercise application on performance-related physical fitness outcomes and selected health indicators in healthy young adults. A total of 78 participants are randomly assigned to a conventional exercise group (n = 26), a mobile application-based exercise group (n = 26), or a control group (n = 26). Both intervention groups complete an identical six-week high-intensity interval training (HIIT) program, either supervised or delivered via the 7-Minute Workout® mobile application. The control group receives no intervention. Pre- and post-intervention assessments include muscular endurance (curl-ups, push-ups), lower extremity anaerobic power (vertical jump), and hamstring and lower back flexibility (sit-and-reach), as well as self-reported sleep quality (Pittsburgh Sleep Quality Index) and pain (Visual Analog Scale).

Trial Health

87
On Track

Trial Health Score

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

Enrollment
78

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Mar 2021

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

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 15, 2021

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 15, 2021

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 15, 2021

Completed
4.6 years until next milestone

First Submitted

Initial submission to the registry

July 18, 2026

Completed
26 days until next milestone

First Posted

Study publicly available on registry

August 13, 2026

Completed
Last Updated

August 13, 2026

Status Verified

August 1, 2026

Enrollment Period

6 months

First QC Date

July 18, 2026

Last Update Submit

August 11, 2026

Conditions

Keywords

Mobile ApplicationsHigh-Intensity Interval TrainingPhysical Fitness

Outcome Measures

Primary Outcomes (4)

  • Physical Fitness Assesment

    Modified Push-up Test

    6 weeks

  • Physical Fitness Assesment

    Curl up

    6 weeks

  • Physical Fitness Assesment

    Vertical Jump Test

    6 weeks

  • Physical Fitness Assesment

    Sit-and-Reach Test

    6 weeks

Secondary Outcomes (2)

  • Sleep Quality

    6 weeks

  • Pain Level

    6 weeks

Study Arms (3)

Control Group

NO INTERVENTION

No intervention was applied to the control group.

Exercise

ACTIVE COMPARATOR

The conventional group performed the high intensity interval training exercise protocol, three times per week for six weeks using printed instructions

Other: Conventional Exercise

Mobile Exercise Group

EXPERIMENTAL

The mobile group was instructed to download the 7-Minute Workout® mobile application and perform the prescribed exercises three times per week for six weeks using the relevant app features.

Behavioral: Exercise

Interventions

ExerciseBEHAVIORAL

The experimental group will utilize the official "7-Minute Workout®" mobile application, developed by the Johnson \& Johnson Human Performance Institute. Based on High-Intensity Circuit Training (HICT) and High-Intensity Interval Training (HIIT) principles, the program consists of 12 alternating bodyweight exercises targeting major muscle groups. Each exercise is performed for 30 seconds, followed by a 10-second rest period. The routine combines aerobic and resistance exercises and includes a 2-minute warm-up and a 3-minute cool-down phase. The app is freely accessible on both Android and iOS platforms.

Also known as: 7 Minute Workout App
Mobile Exercise Group

As described in the American College of Sports Medicine's Health \& Fitness Journal, the core workout consists of 12 bodyweight exercises alternating between major muscle groups. Each exercise is performed for 30 seconds, followed by a 10-second rest period. The training protocol was provided to the participants in a written/text format, containing comprehensive and detailed instructions for each movement. The program includes the following optional warm-up and cool-down protocols: Warm-up exercises (\~2 minutes): Shoulder rolls, arm hugs, standing knee pulls, and standing trunk rotations. Cool-down exercises (\~3 minutes): Seated posterior leg stretches, quadriceps stretches using chair support, arm flexion (upward, forward, and backward), and posterior arm stretches.

Exercise

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Being a university student enrolled in the Department of Physiotherapy and Rehabilitation at Tokat Gaziosmanpaşa University Faculty of Health Sciences
  • Being a healthy individual

You may not qualify if:

  • Having undergone any surgical procedure within the last 6 months
  • Regularly using medication
  • Having any chronic disease
  • Inability to continue the program throughout the study period.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Tokat Gaziosmanpaşa University Health Science Faculty Tokat Turkiye

Tokat Province, Tokat Province, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Sleep Initiation and Maintenance Disorders

Interventions

Exercise

Condition Hierarchy (Ancestors)

Sleep Disorders, IntrinsicDyssomniasSleep Wake DisordersNervous System DiseasesMental Disorders

Intervention Hierarchy (Ancestors)

Motor ActivityMovementMusculoskeletal Physiological PhenomenaMusculoskeletal and Neural Physiological Phenomena

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Doctor of Philosophy, Physical Therapist

Study Record Dates

First Submitted

July 18, 2026

First Posted

August 13, 2026

Study Start

March 15, 2021

Primary Completion

September 15, 2021

Study Completion

December 15, 2021

Last Updated

August 13, 2026

Record last verified: 2026-08

Data Sharing

IPD Sharing
Will share

De-identified individual participant data will be made available upon reasonable request to the corresponding author after the publication of the study.

Shared Documents
ICF
Time Frame
Up to 36 months after publication
Access Criteria
Researchers whose proposed use of the data has been approved by the corresponding author for academic purposes (e.g., meta-analyses or related research). Approved researchers will be granted access to de-identified individual participant data (IPD), along with the Study Protocol, Statistical Analysis Plan (SAP), and Informed Consent Form (ICF). Requests must be submitted via email to the corresponding author. Upon approval, the requested data and documents will be shared securely via email or a secure cloud link.

Locations