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Clinical Trials/NCT07762781
NCT07762781CompletedNot Applicable

Effectiveness Of A Mobile Exercise Application On Sleep, Pain And Physical Fitness In Healthy Adults: A Randomized Controlled Trial

Tokat Gaziosmanpasa University1 site in 1 country78 target enrollmentStarted: March 15, 2021Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
78
Locations
1
Primary Endpoint
Physical Fitness Assesment

Study Overview

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).

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
Single (Participant)

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

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

Exclusion Criteria

  • •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.

Arms & Interventions

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

Intervention: Conventional Exercise (Other)

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.

Intervention: Exercise (Behavioral)

Outcomes

Primary Outcomes

Physical Fitness Assesment

Time Frame: 6 weeks

Modified Push-up Test

Secondary Outcomes

  • Sleep Quality(6 weeks)
  • Pain Level(6 weeks)

Investigators

Sponsor
Tokat Gaziosmanpasa University
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Nilsah YILMAZ

Doctor of Philosophy, Physical Therapist

Tokat Gaziosmanpasa University

Study Sites (1)

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