Impact of a Mobile Exercise Application on Sleep, Pain, and Fitness in Healthy Adults
Effectiveness Of A Mobile Exercise Application On Sleep, Pain And Physical Fitness In Healthy Adults: A Randomized Controlled Trial
1 other identifier
interventional
78
1 country
1
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
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Mar 2021
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
Study Start
First participant enrolled
March 15, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 15, 2021
CompletedStudy Completion
Last participant's last visit for all outcomes
December 15, 2021
CompletedFirst Submitted
Initial submission to the registry
July 18, 2026
CompletedFirst Posted
Study publicly available on registry
August 13, 2026
CompletedAugust 13, 2026
August 1, 2026
6 months
July 18, 2026
August 11, 2026
Conditions
Keywords
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 INTERVENTIONNo intervention was applied to the control group.
Exercise
ACTIVE COMPARATORThe conventional group performed the high intensity interval training exercise protocol, three times per week for six weeks using printed instructions
Mobile Exercise Group
EXPERIMENTALThe 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.
Interventions
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.
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.
Eligibility Criteria
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)
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
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
- 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.
De-identified individual participant data will be made available upon reasonable request to the corresponding author after the publication of the study.