Wearable Monitoring Device in Daily Lives of Community-dwelling Older Adults

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

72 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-07-10

Study Completion Date

2023-07-09

Brief Summary

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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.

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Detailed Description

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Conditions

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Device Ineffective

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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Intervention group

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

Group Type EXPERIMENTAL

Live With Wearable Monitoring Device program

Intervention Type DEVICE

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.

Control group

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

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Live With Wearable Monitoring Device program

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 Type DEVICE

Eligibility Criteria

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Inclusion Criteria

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

Exclusion Criteria

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

Minimum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No