NCT05269303

Brief Summary

The aim is to implement an intervention program to promote the continued use of Wearable Monitoring Devices among older adults through a peer support approach facilitating the incorporation of Wearable Monitoring Devices in daily life.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
72

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Jul 2022

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

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 24, 2022

Completed
11 days until next milestone

First Posted

Study publicly available on registry

March 7, 2022

Completed
4 months until next milestone

Study Start

First participant enrolled

July 10, 2022

Completed
12 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 9, 2023

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 9, 2023

Completed
Last Updated

September 22, 2023

Status Verified

September 1, 2023

Enrollment Period

12 months

First QC Date

February 24, 2022

Last Update Submit

September 20, 2023

Conditions

Device Ineffective

Keywords

community-dwelling older adultsWearable monitoring device

Outcome Measures

Primary Outcomes (1)

  • The change of use intention of wearable monitoring device

    It will be measured using a 4-item, 5-point Likert scale adopted from Bhattacherjee (2001) and Windasari et al. (2021). The five-point scale ranges from 1 = not at all satisfied to 5 = very certain, with higher scores representing a higher chance of continuing to use the WMD.

    Data collection will be conducted at the 1-month (T1), 3-month (T2), and 6-month (T3) time points

Secondary Outcomes (8)

  • The change of adherence rate of wearing wearable monitoring device

    Data collection will be conducted at the 1-month (T1), 3-month (T2), and 6-month (T3) time points

  • The change in quality of life among baseline (T0) and at the 1-month (T1), 3-month (T2), and 6-month (T3) time points

    baseline (T0) and at the 1-month (T1), 3-month (T2), and 6-month (T3) time points

  • The change of health service utilization among baseline (T0) and at the 1-month (T1), 3-month (T2), and 6-month (T3) time points

    baseline (T0) and at the 1-month (T1), 3-month (T2), and 6-month (T3) time points

  • Recruitment rate

    baseline pre-intervention

  • Attrition rate

    6-month (T3) time points

  • +3 more secondary outcomes

Study Arms (2)

Intervention group

EXPERIMENTAL

Participants will receive a 3-month Live With Wearable Monitoring Device program.

Device: Live With Wearable Monitoring Device program

Control group

NO INTERVENTION

Usual care. As with the participants in the intervention group, those in the control group can utilize the features in the Wearable Monitoring Device.

Interventions

Live With Wearable Monitoring Device programDEVICE

The participants in the intervention group will receive a home visit by a Community Healthcare Worker in the first month, and biweekly motivational messages via Whats App in the second and third months.

Intervention group

Eligibility Criteria

Age60 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • aged 60 or above
  • own a smartphone
  • able to communicate in Cantonese or Mandarin
  • able to access the Internet at home or elsewhere

You may not qualify if:

  • have a confirmed diagnosis of cognitive impairment
  • bed-bound
  • currently own a wearable monitoring device
  • have already engaged in other wearable device studies

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Siu Sai Wan

Hong Kong, Hong Kong

Location

Related Publications (2)

  • Wong AKC, Bayuo J, Su JJ, Wong FKY, Chow KKS, Wong BP, Wong SM, Hui V. Effectiveness of the Support From Community Health Workers and Health Care Professionals on the Sustained Use of Wearable Monitoring Devices Among Community-Dwelling Older Adults: Feasibility Randomized Controlled Trial. J Med Internet Res. 2024 Nov 18;26:e52435. doi: 10.2196/52435.

    PMID: 39556810DERIVED

  • Wong AKC, Tso WC, Su JJ, Hui VCC, Chow KKS, Wong SM, Wong BB, Wong FKY. Effectiveness of support from community health workers on the sustained use of a wearable monitoring device among community-dwelling older adults: A randomized trial protocol. PLoS One. 2023 Dec 22;18(12):e0294517. doi: 10.1371/journal.pone.0294517. eCollection 2023.

    PMID: 38134126DERIVED

Study Officials

  • Arkers Wong, Ph.D.

    The Hong Kong Polytechnic University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant professor

Study Record Dates

First Submitted

February 24, 2022

First Posted

March 7, 2022

Study Start

July 10, 2022

Primary Completion

July 9, 2023

Study Completion

July 9, 2023

Last Updated

September 22, 2023

Record last verified: 2023-09

Data Sharing

IPD Sharing
Will not share

Locations

HK(1)