The Effects of 8-week Resistance and Aerobic Exercise on Anxiety, Depression, Sleep, Inhibitory Control in Young Adults With Smartphone Overdependence
1 other identifier
interventional
36
1 country
1
Brief Summary
The purpose of this study is to identify the effects of the resistance exercise and aerobic exercise on depression, anxiety, sleep, inhibitory control in young adult with smartphone overdependence
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jan 2025
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
January 6, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 4, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
February 5, 2025
CompletedFirst Submitted
Initial submission to the registry
February 9, 2025
CompletedFirst Posted
Study publicly available on registry
February 27, 2025
CompletedFebruary 27, 2025
February 1, 2025
29 days
February 9, 2025
February 21, 2025
Conditions
Outcome Measures
Primary Outcomes (5)
sleep duration
In this study, we will assess participants' sleep duration using a wrist-worn GENEActiv triaxial accelerometer (Activinsights, Cambridge, UK). Participants will be instructed to wear the device on their non-dominant wrist 24 hours a day for 8 days, except during contact sports that may pose a risk of injury. Sleep duration (minutes) is defined as the total time spent sleeping.
pre intervention: for 8days(before the intervention) / post intervention: for 8days(after the intervention)
Sleep efficiency
In this study, we will assess participants' sleep efficiency using a wrist-worn GENEActiv triaxial accelerometer (Activinsights, Cambridge, UK). Participants will be instructed to wear the device on their non-dominant wrist 24 hours a day for 8 days, except during contact sports that may pose a risk of injury. Sleep efficiency(%) is defined as the proportion of time spent asleep relative to time in bed
pre intervention: for 8days(before the intervention) / post intervention: for 8days(after the intervention)
Time in bed
In this study, we will assess participants' time in bed using a wrist-worn GENEActiv triaxial accelerometer (Activinsights, Cambridge, UK). Participants will be instructed to wear the device on their non-dominant wrist 24 hours a day for 8 days, except during contact sports that may pose a risk of injury. Time in bed (minutes) is defined as the total time spent in bed, including both sleep and wakefulness
pre intervention: for 8days(before the intervention) / post intervention: for 8days(after the intervention)
Sleep onset time
In this study, we will assess participants' sleep onset time using a wrist-worn GENEActiv triaxial accelerometer (Activinsights, Cambridge, UK). Participants will be instructed to wear the device on their non-dominant wrist 24 hours a day for 8 days, except during contact sports that may pose a risk of injury. Sleep onset time (hours and minutes) is defined as the time at which sleep begins.
pre intervention: for 8days(before the intervention) / post intervention: for 8days(after the intervention)
wake time
In this study, we will assess participants' sleep onset time using a wrist-worn GENEActiv triaxial accelerometer (Activinsights, Cambridge, UK). Participants will be instructed to wear the device on their non-dominant wrist 24 hours a day for 8 days, except during contact sports that may pose a risk of injury. Wake time (hours and minutes) is defined as the final wake-up time.
pre intervention: for 8days(before the intervention) / post intervention: for 8days(after the intervention)
Secondary Outcomes (3)
Depression
pre intervention(day 1), post intervention(day 57)
Anxiety
pre intervention(day 1), post intervention(day 57)
Inhibition
pre intervention(day 1), post intervention(day 57)
Study Arms (3)
resistance exercise group
EXPERIMENTALThey will perform resistance exercise for 8 weeks.
aerobic exercise group
EXPERIMENTALThey will perform aerobic exercise for 8 weeks.
control group
SHAM COMPARATORThey will maintain their usual lifestyle for 8 weeks.
Interventions
Participants will perform resistance exercise for 8 weeks
Participants will perform aerobic exercise for 8 weeks
Eligibility Criteria
You may qualify if:
- Smartphone overdependent scale score of 24 ≥
- No regular exercise in the past 3 months
You may not qualify if:
- Unable to perform exercise
- Patients with musculoskeletal disorders
- Patients with cardiovascular diseases.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of Seoul, Centennial Memorial Hall.
Dongdaemun, Seoul, South Korea
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, INVESTIGATOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- University of Seoul
Study Record Dates
First Submitted
February 9, 2025
First Posted
February 27, 2025
Study Start
January 6, 2025
Primary Completion
February 4, 2025
Study Completion
February 5, 2025
Last Updated
February 27, 2025
Record last verified: 2025-02
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL, ICF
- Time Frame
- 2025.03.01\~2026.03.01
Study Protocol, Informed Consent Form (ICF)