NCT06848322

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

87
On Track

Trial Health Score

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

Enrollment
36

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jan 2025

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

January 6, 2025

Completed
29 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 4, 2025

Completed
1 day until next milestone

Study Completion

Last participant's last visit for all outcomes

February 5, 2025

Completed
4 days until next milestone

First Submitted

Initial submission to the registry

February 9, 2025

Completed
18 days until next milestone

First Posted

Study publicly available on registry

February 27, 2025

Completed
Last Updated

February 27, 2025

Status Verified

February 1, 2025

Enrollment Period

29 days

First QC Date

February 9, 2025

Last Update Submit

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

EXPERIMENTAL

They will perform resistance exercise for 8 weeks.

Behavioral: resistance exercise

aerobic exercise group

EXPERIMENTAL

They will perform aerobic exercise for 8 weeks.

Behavioral: aerobic exercise

control group

SHAM COMPARATOR

They will maintain their usual lifestyle for 8 weeks.

Other: Control (placebo)

Interventions

Participants will perform resistance exercise for 8 weeks

Also known as: aerobic exercise, control
resistance exercise group

Participants will perform aerobic exercise for 8 weeks

aerobic exercise group

Participants will maintain their usual lifestyle for 8 weeks.

control group

Eligibility Criteria

Age20 Years - 29 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

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

Location

MeSH Terms

Conditions

Motor ActivityInternet Addiction DisorderInhibition, Psychological

Interventions

Resistance TrainingExercise

Condition Hierarchy (Ancestors)

BehaviorTechnology AddictionBehavior, AddictiveCompulsive BehaviorImpulsive Behavior

Intervention Hierarchy (Ancestors)

Exercise TherapyRehabilitationAftercareContinuity of Patient CarePatient CareTherapeuticsPhysical Therapy ModalitiesPhysical Conditioning, HumanMotor ActivityMovementMusculoskeletal Physiological PhenomenaMusculoskeletal and Neural Physiological Phenomena

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, INVESTIGATOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: resistance exercise group → Experimental aerobic exercise group → Experimental control → No Intervention There are three groups in this study: the resistance exercise group, the aerobic exercise group, and the control group. Measurements are conducted at three time points: pre-intervention, mid-intervention (4 weeks after the intervention), and post-intervention
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

Study Protocol, Informed Consent Form (ICF)

Shared Documents
STUDY PROTOCOL, ICF
Time Frame
2025.03.01\~2026.03.01

Locations