- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05636982
A Telecare-based Intervention in Reducing Stress Level of Informal Caregivers of Community-dwelling Older Adults
Effectiveness of a Telecare-based Intervention Programme in Supporting the Informal Caregivers of Community-dwelling Older Adults in Reducing Stress Level: Study Protocol for a Pilot Randomized Controlled Trial
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Objectives: The primary caregivers of older adults provide intimate and immediate support when their loved one is in urgent need. Due to the full-time commitment in a caregiving role, the caregiver may not have extra time to join the onsite community services that are available to them in the daytime. With the support of advanced technology, telecare seems to be a convenient and easily accessible channel to provide individualized caregiving advice to the caregivers. This study examines the effectiveness of a telecare-based intervention programme for caregivers.
Hypothesis to be tested: To test if the research team-developed telecare-based intervention programme is effective in reducing the stress level of caregivers.
Design and subjects: This is a single-blinded, two-armed pilot randomized controlled trial. The subjects are people who are aged 18 or above, provide care to older adults aged ≥ 60 at least 4 hours per week for a minimum of 3 months, are capable to use smartphone to access the Internet, and are without psychiatric illnesses and cognitive impairment.
Interventions: The intervention group receives the telecare intervention programme designed by the research team. The caregivers receive nurse case management supported by a community health-social service team and be able to access a peer-support discussion forum. The control group receives usual community services
Primary outcome measure: Self-reported stress level; secondary outcome measures: self-efficacy, depression level, quality of life, and caregiving burden.
Data analysis: independent t-test or Mann-Whitney U test will be used to determine the group differences in outcomes measurements between pre- and post-intervention. Intention-to-treat will be employed as the primary analysis in this study. Per-protocol (PP) analysis will be adopted as the secondary analysis and performed separately.
Expected outcomes: Caregivers in the intervention group would benefit from the telecare-based programme with reduced stress level, depression level and caregiving burdens and yet enhanced self-efficacy and quality of life.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Kowloon, Hong Kong
- Salvation Army
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- people who are aged ≥18 years old
- understand and communicate in Cantonese
- provide care to the older adults aged ≥60 at least 4 hours per week for a minimum of 3 months
- smartphone user and know how to access the Internet
- commit to attend bi-weekly, 15-30mins online meetings with the program providers over the 3-month period
- willing to receive individual-specific video messages covering caregiving skills via WhatsApp
Exclusion Criteria:
- alcoholic drinkers or psychiatric drug users
- illiterate (inability to write and read)
- having psychiatric problems
- having cognitive impairment as evidenced by scoring 22 or above in Hong Kong version of Montreal Cognitive Assessment
- already participated in other telecare health or social programs
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Telecare-based intervention program
This group of participants will receive a 3-month telecare-based intervention program which includes three main components: 1) online nurse case management supported by a health-social partnership team, 2) individual-specific video messages covering caregiving skills via WhatsApp, and 3) online information center and discussion forum via a password-protected, newly-developed caregiver website.
|
A 3-month telecare-based intervention program
|
|
No Intervention: Control
The control group will receive conventional community services.
The caregiver will attend five educational sessions that covers caregiving skills in the community centers on a fixed schedule.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Stress level
Time Frame: 3-month
|
Stress level will be measured by the 14-item Chinese version of Perceived Stress Scale (PSS).
It has been applied extensively to measure the degree of perceived stress for informal caregivers.
The total score ranges between 0 (minimum stress perceived) and 56 (maximum stress perceived), with a higher score representing a greater perceived stress level.
|
3-month
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Self-efficacy
Time Frame: 3-month
|
The General Self-Efficacy Scale (CGSE) will be used to assess the self-perceived ability to cope with stressful life events.
The Chinese version of CGSE contains 10 items and is scored on a 4-point Likert scale ranging from 1 (not at all true) to 4 (exactly true).
The total score ranges from 10 to 40, with higher scores indicating a greater belief in one's competence to deal with difficulties.
|
3-month
|
|
Depression
Time Frame: 3-month
|
Depression level will be measured by the Chinese version of The Center for Epidemiologic Studies Depression Scale (CES-D).
The CES-D is a self-reported scale that measures the presence of depressive symptoms.
This 4-point scale is a 20-item instrument.
The total scores ranged from 0 to 60, with higher scores indicating more depressive symptoms.
|
3-month
|
|
Quality of life (general well-being of individual)
Time Frame: 3-month
|
The Chinese (HK) version (SF-12v2-HK) of 12-item Short Form Health Survey version 2 will be used to assess the quality of life of the informal caregivers.
The questionnaire contains 12 items involving different domains of health concepts, which include physical functioning, role limitation due to emotional problems, role limitation due to physical problems, mental health scale, general health, bodily pain, and social functioning and vitality (energy/fatigue).
The scale ranged from 0 to 100, with 50 indicating the standardized norm scale.
|
3-month
|
|
Caregiving burden
Time Frame: 3-month
|
Caregiving burden will be measured using the Zarit Burden Interview (ZBI).
It contains 22 items and is scored on a 5-point Likert scale ranging from 0 (never) to 4 (nearly always).
The total score ranges from 0 to 88, with a score of 24 or above may indicate a higher chance of developing depression.
|
3-month
|
Collaborators and Investigators
Investigators
- Principal Investigator: Arkers Wong, PhD, The Hong Kong Polytechnic University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- P0038343
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Telemedicine
-
Michigan State UniversityUniversity of Michigan; Wake Forest University Health Sciences; Babes-Bolyai...CompletedUsual Care | Telemedicine: Smoking Cessation App Only | Telemedicine: Smoking Cessation Counseling | Telemedicine: App + CounselingRomania
-
Attune Health Research, Inc.Rheumatology Research FoundationRecruiting
-
University Hospital, Basel, SwitzerlandInnosuisse - Swiss Innovation AgencyCompleted
-
Wake Forest University Health SciencesCompleted
-
National University Health System, SingaporeCompletedTelemedicineSingapore
-
CochlearCompletedTelemedicineUnited States
-
Wake Forest University Health SciencesCompleted
-
Buzzi Children's HospitalCompleted
-
The Hong Kong Polytechnic UniversityCompleted
Clinical Trials on Telecare-based intervention program
-
National Taiwan University HospitalNational Health Research Institutes, Taiwan; National Taiwan UniversityCompleted
-
National Taiwan University HospitalNational Science Council, TaiwanCompleted
-
Fidan BalkayaInonu UniversityActive, not recruitingMOBILE WEB-BASED INTERVENTION PROGRAM | NURSING EDUCATION STRESS | SLEEP QUALITYTurkey (Türkiye)
-
Inonu UniversityTuba UçarCompleted
-
TC Erciyes UniversityKayseri City HospitalNot yet recruitingCoronary Artery Disease (CAD)Turkey (Türkiye)
-
University of UtahNational Cancer Institute (NCI)CompletedColorectal CancerUnited States
-
Marmara UniversityNot yet recruitingSexual Arousal Disorder | Sexual Desire Disorder
-
Washington University School of MedicineUniversity of Southern CaliforniaCompletedPremature Birth of NewbornUnited States
-
Gazi UniversityCompleted
-
Indiana UniversityNational Center for Advancing Translational Sciences (NCATS)TerminatedChronic Pain | Opioid DependenceUnited States