NCT06739876

Brief Summary

The goal of this randomized controlled trial is to examine whether the use of a wearable device and social media based intention increases physical activity and enhance sleep quality among adults.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
75

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Mar 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

First Submitted

Initial submission to the registry

December 12, 2024

Completed
6 days until next milestone

First Posted

Study publicly available on registry

December 18, 2024

Completed
3 months until next milestone

Study Start

First participant enrolled

March 5, 2025

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2025

Completed
11 months until next milestone

Results Posted

Study results publicly available

April 29, 2026

Completed
Last Updated

April 29, 2026

Status Verified

April 1, 2026

Enrollment Period

3 months

First QC Date

December 12, 2024

Results QC Date

March 19, 2026

Last Update Submit

April 8, 2026

Conditions

Keywords

Sleep qualitywearable devicemotivationsocial media supportphysical activity

Outcome Measures

Primary Outcomes (1)

  • Changes in Physical Activity

    Change in physical activity will be assessed by self-report measure on sedentary breaks and behaviour (the measure was developed by the investigator in a previous study). In addition, it will also be assessed by a measurable device (physical activity-related parameters assessed by Garmin monitor).

    Baseline, and post-assessment (immediately after the intervention), one month follow-up

Secondary Outcomes (1)

  • Changes in Sedentary Behavior

    Baseline, and post-assessment (immediately after the intervention), one month follow-up

Study Arms (3)

No wearable device: Control

NO INTERVENTION

The control group will not wear the device at times other than completing assessments at baseline, post-intervention, and follow-up.

Intervention: Device and motivational support via social media

EXPERIMENTAL

Participants in the Device and motivational support group will wear the device (Garmin tracker) for a month. In addition, they will receive motivational support via social media.

Behavioral: Wearable device-based intervention (with motivational support via social media)

Intervention: Device

EXPERIMENTAL

Participants in the Device group will wear the device (Garmin tracker) for a month.

Behavioral: Wearable device-based intervention (without support)

Interventions

The wearable device-based intervention aims to reduce sedentary behavior as the Move alert function may facilitate the management of one's physical activity. Motivational support will be provided via an online community created using LINE platform. The platform serve for the following purposes: a) providing psychoeduation prior to the intervention; b) providing a place for participants to motivate and encourage each other; c) provide health knowledge to participants weekly, to motivate behavioral change; d) encouraging participants to upload their daily step count to the community page to motivate each other's progress; e) based on participant's performance, research assistants will provide tailored support using Line stickers designed for the present intervention; f) research assistants will monitor participants' step counts and provide prizes (vouchers) for those who had the most step counts and made the most improvements.

Intervention: Device and motivational support via social media

The wearable device-based intervention aims to reduce sedentary behavior as the Move alert function may facilitate the management of one's physical activity.

Intervention: Device

Eligibility Criteria

Age18 Years - 64 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Those who have not used a wearable-device before.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

National Chung Hsing University

Taichung, 402, Taiwan

Location

MeSH Terms

Conditions

Motor ActivitySleep Initiation and Maintenance Disorders

Condition Hierarchy (Ancestors)

BehaviorSleep Disorders, IntrinsicDyssomniasSleep Wake DisordersNervous System DiseasesMental Disorders

Limitations and Caveats

The study was conducted at a single university using convenience sampling. The relatively small sample size and short intervention period may limit the generalizability of the findings.

Results Point of Contact

Title
Po-Wen Ku
Organization
Naitonal Chung Hsing University

Publication Agreements

PI is Sponsor Employee
No
Restrictive Agreement
No

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
PREVENTION
Intervention Model
PARALLEL
Model Details: Participants in the intervention group will wear a device and will either receive motivational support via social media or not. The control group will not wear a device during the intervention phase.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor

Study Record Dates

First Submitted

December 12, 2024

First Posted

December 18, 2024

Study Start

March 5, 2025

Primary Completion

June 1, 2025

Study Completion

June 1, 2025

Last Updated

April 29, 2026

Results First Posted

April 29, 2026

Record last verified: 2026-04

Data Sharing

IPD Sharing
Will not share

Individual participant data will not be shared with other researchers. The informed consent form signed by participants did not include provisions for data sharing outside of the study team. Therefore, we are not authorized to make the individual-level data available for secondary use.

Locations