Caregiver BurdenNCT06604481
An Online Ecoaching RCT Intervention for Carers: Enhancing Wellbeing and Resilience Through Self-Help Strategies
A study testing eCoaching for Caregivers of Older Adults and eCoaching (need specific) for Caregivers of Older Adults in people with Caregiver Burden and Self Efficacy, run by The University of Hong Kong at 1 site in Hong Kong.
Trial summary
The goal of this three-armed, double-blind randomized controlled trial (RCT) is to compare the effectiveness of an online self-help eCoaching intervention designed for caregivers. Read more about this study
- Who is it for?
- Ages 18 years and olderHealthy volunteers can take part
- Conditions the study is for
- Caregiver Burden, Self Efficacy, Quality of Life
- What is being tested?
- eCoaching for Caregivers of Older Adults and eCoaching (need specific) for Caregivers of Older Adults
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 232 participants
- Where
- 1 siteHong Kong
- Study dates
- 30 Apr 2025to Sep 2026
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- being an adult aged 18 or above with a family member aged 60 or above requiring caregiving, providing at least 6 hours of care per week
- self-identifying as a family caregiver
- living in Hong Kong
- able to communicate with the interventionist
- voluntary participation
- reporting mild risk need in Carer Need Screening tool
Who cannot join
- having diagnosed Alzheimer's or other dementia
- experiencing acute health conditions that hinder caregiving support or intervention participation
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Hong Kong1 site, 1 recruiting
- Recruiting
Sau Po Center on Ageing HKU
Hong Kong
About this study
Official title: Randomized Controlled Trial to Test the Efficacy of Online Ecoaching to Support Caregivers of Older Adults in Hong Kong: Enhancing Carers' Wellbeing and Resilience
The goal of this three-armed, double-blind randomized controlled trial (RCT) is to compare the effectiveness of an online self-help eCoaching intervention designed for caregivers. The main questions it aims to answer are:
What is the impact of the online self-help eCoaching intervention on the well-being, depressive symptoms, and self-efficacy of participants? Researchers will compare the results between the intervention groups and the control group to see if participants in the intervention groups have lower distress, burden and higher accuracy.
Read the detailed description
Proposed Study:
The investigators propose a 6-week randomized controlled trial to compare the effectiveness of a novel online self-help intervention for caregivers of older adults in Hong Kong. The intervention is based on Cognitive Behavioral Therapy, lifestyle intervention, and effective communication skills.
Randomization:
The research team will perform individual randomization using statistical software R. Randomization will be using random permuted blocks via an online computer randomization system from an independent clinical trials unit. Participants will be randomized into two intervention groups or control group.
Outcomes:
The primary objective of this study is to evaluate the effectiveness of an online self-help eCoaching intervention that incorporates symptom management, stress management, and coping skills training in promoting healthy behavior change among caregivers. Additionally, this study aims to investigate the effectiveness of the online self-help eCoaching intervention in reducing carers' depressive symptoms and anxiety. Another key objective is to enhance carers' self-efficacy for stress management and resilience by equipping them with the necessary skills and strategies provided through the eCoaching intervention.
Recruitment and Inclusion Criteria:
A total of 232 caregivers from seven district-based caregiver support units will be recruited. The inclusion criteria are as follows: 1) Participants must be adults aged 18 or above with a family member aged 60 or above requiring caregiving, providing at least 6 hours of care per week; 2) They must self-identify as a family caregiver; 3) Participants must live in Hong Kong and 4) be able to communicate with the interventionist; 5) Participation must be voluntary; 6) Additionally, participants must report mild need in the Carer multidimensional Need Assessment tool. The exclusion criteria include: 1) having diagnosed Alzheimer's or other dementia; or 2) experiencing acute health conditions that hinder caregiving support or intervention participation.
Study Procedures:
This study will consist of a 6-week intervention, with a screening process to be conducted prior to the intervention implementation. Baseline and immediately after the intervention, as well as a 3-month follow-up assessment, will be performed for statistical comparison. The participation of caregivers in tests, surveys, and interviews will not affect the quality of care they receive. No drug usage or medical treatment is involved in this study, and there are no anticipated physical or medical risks to participants. Withdrawal from the study is voluntary at any time, and will not impact participants' ongoing medical care or legal rights.
The screening process involves carers completing a standardized screening form comprising items pertaining to demographics, self-efficacy, caregiving preparedness, and willingness to join, which they will either fill out independently or have facilitated by project staff upon enrolling for membership. Carers' needs are classified into four levels: low, mild, moderate, and high.
The Carer Multidimensional Need Assessment Tool was developed and validated by the research team of the Jockey Club Carer Space Project, which was led by Professor Vivian Lou, the Director of the Sau Po Centre on Ageing at the University of Hong Kong. The research centre followed a six-step approach, based on the scale development method proposed by Hinkin (1995), to establish the Carer Need Screening Tool. These steps encompassed: (1) a literature review, (2) the formation of an expert panel, (3) a Delphi study, (4) the confirmation of an item list, (5) an item validation study, and (6) the finalization of the scale. The research team developed a 22-item screening tool, and the screening tool involves 5 domains of risk including carers' mental ill health, caregiving capacity, lack of support, carers' health challenges, and high care demands.
Data Analysis:
A MANOVA will be conducted for the continuous variables and a chi-square test will be used for the categorical variables, to compare the differences between the primary and secondary outcomes of the three groups. The associations among different variables will be investigated using Pearson's correlation analysis. The interaction Group x Time treatment effects within and between the groups (eCoaching I, eCoaching II, Control) will be tested with a factorial ANOVA with repeated measures. Differential changes in each outcome across the 3 assessment time points (T0, T1, T2) between the three treatment groups will be compared. Recruitment rate, attrition rate, and missing data will also be examined and reported. All outcome measures will be analysed based on intention-to-treat principles. Exploratory analysis will assess whether the intervention effects are mediated by caregiver self-efficacy or knowledge gain. The data will be analysed using SPSS, version 28.0. All statistical tests will be two-sided with the level of significance set at .05.
Data Storage and Privacy:
Personal data will be securely stored by the principal investigator for 5 years after the publication of the first paper, followed by 10 years for anonymized data. All information will be used for research purposes only and stored on encrypted workstations and password-protected online cloud storage.
- Conditions
- Caregiver Burden, Self Efficacy, Quality of Life, Anxiety Depression, Resilience
- Being tested
- eCoaching for Caregivers of Older Adults, eCoaching (need specific) for Caregivers of Older Adults, Control Intervention for Caregivers of Older Adults
- Medical subject headings
- Caregiver Burden
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
eCoaching for Caregivers of Older AdultsBehavioural
The experimental group receives an online intervention based on Cognitive Behavioral Therapy, Dialectical Behavioral Therapy, lifestyle intervention, and effective communication skills. This program is designed to operate individually on an e-platform. It consists of 6 weekly sessions, each lasting for less than 90 minutes. The content of the sessions focuses on teaching caregivers CBT techniques, lifestyle modifications to improve caregiving experiences, and effective communication strategies. In between each session, participants are assigned home practices to reinforce the skills learned further. All content will be included.
eCoaching (need specific) for Caregivers of Older AdultsBehavioural
The experimental group receives an online intervention based on Cognitive Behavioral Therapy, Dialectical Behavioral Therapy, lifestyle intervention, and effective communication skills as in eCoaching I. However, eCoaching II will include content specified to carer's specific need.
Control Intervention for Caregivers of Older AdultsBehavioural
The control group attends 6 weekly online sessions that primarily provide educational information about lifestyle factors and communication. These sessions aim to enhance the control group's knowledge and understanding of the factors that impact caregiving. Each session in the control group also lasts for 90 minutes. The focus of these activities will be on building practical caregiving skills and promoting overall well-being, rather than targeting any particular psychological or mental health-related factors directly.
| Study group | Role | What they receive |
|---|---|---|
| eCoaching Group I | Experimental | Online intervention based on Cognitive Behavioral Therapy, Dialectical Behavioral Therapy, lifestyle intervention, and effective communication skills. All content will be covered. Receives: Behavioral: eCoaching for Caregivers of Older Adults |
| eCoaching Group II | Experimental | Online intervention based on Cognitive Behavioral Therapy, Dialectical Behavioral Therapy, lifestyle intervention, and effective communication skills. Content will be covered specified to the carer's specific needs. Receives: Behavioral: eCoaching (need specific) for Caregivers of Older Adults |
| Control Group | Active comparator | Online sessions focused on education about lifestyle and communication. Receives: Behavioral: Control Intervention for Caregivers of Older Adults |
What is being measured
The primary outcome is the main question the study is designed to answer.
Patient Health Questionnaire (PHQ-9)
The PHQ-9 is a self-report instrument used to assess symptoms of depression.
Measured: 3 months
Carers Multidimensional Need Assessment Tool
Carers Multidimensional Need Assessment Tool 22-item. The Carers Multidimensional Need Assessment Tool is a 22-item assessment that evaluates caregivers across 5 key domains of risk:Carers' mental ill health, Caregiving capacity, Lack of support, Carers' health challenges and High care demands.
Measured: 3 months
Generalised Anxiety Disorder (GAD-7)
The GAD-7 is a 7-item screening tool used to assess the severity of generalized anxiety disorder.
Measured: 3 months
Secondary outcomes (4)
Cantonese short version of the Zarit Burden Interview (CZBI)
Reduced burden of caregivers
Measured: 3 months
The World Health Organization Quality of Life (WHOQoL-BREF)
The WHOQOL-BREF is a 28-item instrument developed by the World Health Organization to assess an individual's quality of life across four domains: physical health, psychological health, social relationships, and environment.
Measured: 3 months
Connor-Davidson Resilience Scale (CD-RISC-25)
The CD-RISC is a 25-item self-administered scale that assesses an individual's level of resilience.
Measured: 3 months
Self-Care Self-Efficacy Scale (SCSES-10)
The SCSES-10 is a measurement tool used to assess an individual's self-efficacy self-care self-efficacy for chronic illness and has been tested in the Hong Kong population.
Measured: 3 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted19 Sep 2024
- Study start30 Apr 2025
- Primary completionSep 2026 (estimated)
- Study completionSep 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Caregiver BurdenStudies of the same condition, open and under way.
- More trials run by The University of Hong KongThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Supportive care
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind
- Who is masked
- Participant, Outcomes assessor
- Enrolment
- 232 participants (estimated)
Sponsor and investigators
- Lead sponsor
- The University of Hong Kong
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Prof. Vivian W.Q. Lou, The University of Hong Kong
- Investigators
- Vivian Lou, PhD, Principal investigator, Sau Po Center on Ageing, HKU
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06604481
- Sponsor's protocol ID
- 2023-0030-001-e
- Status last verified
- Jun 2025
- First submitted
- 17 Sep 2024
- Last updated
- 10 Jun 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: Data collected in this study will be published and submitted to academic journals to share with other researchers.
Publications
Tsoi TCW, Kwok KYH, Chan WS, Tang VMY, Chandola T, Quan J, Yu CY, Lou VW. An e-Coaching Intervention for Family Carers to Enhance Well-Being and Resilience Through Self-Help Strategies: Protocol for a Randomized Controlled Trial. JMIR Res Protoc. 2026 May 27;15:e75944. doi: 10.2196/75944.
PubMed 42227577
Study at a glance
From the registry record, last updated by the sponsor on 10 Jun 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Randomized Controlled Trial to Test the Efficacy of Online Ecoaching to Support Caregivers of Older Adults in Hong Kong: Enhancing Carers' Wellbeing and Resilience
- ClinicalTrials.gov ID
- NCT06604481
- Acronym / sponsor ID
- 2023-0030-001-e
- Conditions
- Caregiver Burden, Self Efficacy, Quality of Life, Anxiety Depression, Resilience
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 232 participants (estimated)
- Lead sponsor
- The University of Hong KongUniversity, hospital or other
- Study start
- 30 Apr 2025 (actual)
- Primary completion
- Sep 2026 (estimated)
- Study completion
- Sep 2026 (estimated)
- First posted
- 19 Sep 2024 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The goal of this three-armed, double-blind randomized controlled trial (RCT) is to compare the effectiveness of an online self-help eCoaching intervention designed for caregivers. The main questions it aims to answer are:
What is the impact of the online self-help eCoaching intervention on the well-being, depressive symptoms, and self-efficacy of participants? Researchers will compare the results between the intervention groups and the control group to see if participants in the intervention groups have lower distress, burden and higher accuracy.
Detailed description
Proposed Study:
The investigators propose a 6-week randomized controlled trial to compare the effectiveness of a novel online self-help intervention for caregivers of older adults in Hong Kong. The intervention is based on Cognitive Behavioral Therapy, lifestyle intervention, and effective communication skills.
Randomization:
The research team will perform individual randomization using statistical software R. Randomization will be using random permuted blocks via an online computer randomization system from an independent clinical trials unit. Participants will be randomized into two intervention groups or control group.
Outcomes:
The primary objective of this study is to evaluate the effectiveness of an online self-help eCoaching intervention that incorporates symptom management, stress management, and coping skills training in promoting healthy behavior change among caregivers. Additionally, this study aims to investigate the effectiveness of the online self-help eCoaching intervention in reducing carers' depressive symptoms and anxiety. Another key objective is to enhance carers' self-efficacy for stress management and resilience by equipping them with the necessary skills and strategies provided through the eCoaching intervention.
Recruitment and Inclusion Criteria:
A total of 232 caregivers from seven district-based caregiver support units will be recruited. The inclusion criteria are as follows: 1) Participants must be adults aged 18 or above with a family member aged 60 or above requiring caregiving, providing at least 6 hours of care per week; 2) They must self-identify as a family caregiver; 3) Participants must live in Hong Kong and 4) be able to communicate with the interventionist; 5) Participation must be voluntary; 6) Additionally, participants must report mild need in the Carer multidimensional Need Assessment tool. The exclusion criteria include: 1) having diagnosed Alzheimer's or other dementia; or 2) experiencing acute health conditions that hinder caregiving support or intervention participation.
Study Procedures:
This study will consist of a 6-week intervention, with a screening process to be conducted prior to the intervention implementation. Baseline and immediately after the intervention, as well as a 3-month follow-up assessment, will be performed for statistical comparison. The participation of caregivers in tests, surveys, and interviews will not affect the quality of care they receive. No drug usage or medical treatment is involved in this study, and there are no anticipated physical or medical risks to participants. Withdrawal from the study is voluntary at any time, and will not impact participants' ongoing medical care or legal rights.
The screening process involves carers completing a standardized screening form comprising items pertaining to demographics, self-efficacy, caregiving preparedness, and willingness to join, which they will either fill out independently or have facilitated by project staff upon enrolling for membership. Carers' needs are classified into four levels: low, mild, moderate, and high.
The Carer Multidimensional Need Assessment Tool was developed and validated by the research team of the Jockey Club Carer Space Project, which was led by Professor Vivian Lou, the Director of the Sau Po Centre on Ageing at the University of Hong Kong. The research centre followed a six-step approach, based on the scale development method proposed by Hinkin (1995), to establish the Carer Need Screening Tool. These steps encompassed: (1) a literature review, (2) the formation of an expert panel, (3) a Delphi study, (4) the confirmation of an item list, (5) an item validation study, and (6) the finalization of the scale. The research team developed a 22-item screening tool, and the screening tool involves 5 domains of risk including carers' mental ill health, caregiving capacity, lack of support, carers' health challenges, and high care demands.
Data Analysis:
A MANOVA will be conducted for the continuous variables and a chi-square test will be used for the categorical variables, to compare the differences between the primary and secondary outcomes of the three groups. The associations among different variables will be investigated using Pearson's correlation analysis. The interaction Group x Time treatment effects within and between the groups (eCoaching I, eCoaching II, Control) will be tested with a factorial ANOVA with repeated measures. Differential changes in each outcome across the 3 assessment time points (T0, T1, T2) between the three treatment groups will be compared. Recruitment rate, attrition rate, and missing data will also be examined and reported. All outcome measures will be analysed based on intention-to-treat principles. Exploratory analysis will assess whether the intervention effects are mediated by caregiver self-efficacy or knowledge gain. The data will be analysed using SPSS, version 28.0. All statistical tests will be two-sided with the level of significance set at .05.
Data Storage and Privacy:
Personal data will be securely stored by the principal investigator for 5 years after the publication of the first paper, followed by 10 years for anonymized data. All information will be used for research purposes only and stored on encrypted workstations and password-protected online cloud storage.
Study design
- Primary purpose
- Supportive care
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (participant, outcomes assessor)
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| eCoaching Group I | Experimental | Behavioral: eCoaching for Caregivers of Older AdultsOnline intervention based on Cognitive Behavioral Therapy, Dialectical Behavioral Therapy, lifestyle intervention, and effective communication skills. All content will be covered. |
| eCoaching Group II | Experimental | Behavioral: eCoaching (need specific) for Caregivers of Older AdultsOnline intervention based on Cognitive Behavioral Therapy, Dialectical Behavioral Therapy, lifestyle intervention, and effective communication skills. Content will be covered specified to the carer's specific needs. |
| Control Group | Active comparator | Behavioral: Control Intervention for Caregivers of Older AdultsOnline sessions focused on education about lifestyle and communication. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (6 listed)
- being an adult aged 18 or above with a family member aged 60 or above requiring caregiving, providing at least 6 hours of care per week
- self-identifying as a family caregiver
- living in Hong Kong
- able to communicate with the interventionist
- voluntary participation
Key exclusion criteria (2 listed)
- having diagnosed Alzheimer's or other dementia
- experiencing acute health conditions that hinder caregiving support or intervention participation
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| eCoaching for Caregivers of Older AdultsThe experimental group receives an online intervention based on Cognitive Behavioral Therapy, Dialectical Behavioral Therapy, lifestyle intervention, and effective communication skills. This program is designed to operate individually on an e-platform. It consists of 6 weekly sessions, each lasting for less than 90 minutes. The content of the sessions focuses on teaching caregivers CBT techniques, lifestyle modifications to improve caregiving experiences, and effective communication strategies. In between each session, participants are assigned home practices to reinforce the skills learned further. All content will be included. | Behavioural | eCoaching Group I |
| eCoaching (need specific) for Caregivers of Older AdultsThe experimental group receives an online intervention based on Cognitive Behavioral Therapy, Dialectical Behavioral Therapy, lifestyle intervention, and effective communication skills as in eCoaching I. However, eCoaching II will include content specified to carer's specific need. | Behavioural | eCoaching Group II |
| Control Intervention for Caregivers of Older AdultsThe control group attends 6 weekly online sessions that primarily provide educational information about lifestyle factors and communication. These sessions aim to enhance the control group's knowledge and understanding of the factors that impact caregiving. Each session in the control group also lasts for 90 minutes. The focus of these activities will be on building practical caregiving skills and promoting overall well-being, rather than targeting any particular psychological or mental health-related factors directly. | Behavioural | Control Group |
Primary outcome
Patient Health Questionnaire (PHQ-9)
Time frame: 3 months
The PHQ-9 is a self-report instrument used to assess symptoms of depression.
Carers Multidimensional Need Assessment Tool
Time frame: 3 months
Carers Multidimensional Need Assessment Tool 22-item. The Carers Multidimensional Need Assessment Tool is a 22-item assessment that evaluates caregivers across 5 key domains of risk:Carers' mental ill health, Caregiving capacity, Lack of support, Carers' health challenges and High care demands.
Generalised Anxiety Disorder (GAD-7)
Time frame: 3 months
The GAD-7 is a 7-item screening tool used to assess the severity of generalized anxiety disorder.
4 secondary outcomes
Cantonese short version of the Zarit Burden Interview (CZBI)
Time frame: 3 months
The World Health Organization Quality of Life (WHOQoL-BREF)
Time frame: 3 months
Connor-Davidson Resilience Scale (CD-RISC-25)
Time frame: 3 months
Self-Care Self-Efficacy Scale (SCSES-10)
Time frame: 3 months
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 10 Jun 2025.
- Derived from this study: PubMed 42227577Tsoi TCW, Kwok KYH, Chan WS, Tang VMY, Chandola T, Quan J, Yu CY, Lou VW. An e-Coaching Intervention for Family Carers to Enhance Well-Being and Resilience Through Self-Help Strategies: Protocol for a Randomized Controlled Trial. JMIR Res Protoc. 2026 May 27;15:e75944. doi: 10.2196/75944.
- Individual participant dataSharing planned: Yes. Data collected in this study will be published and submitted to academic journals to share with other researchers.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Vivian Lou, PhD principal investigator
Sau Po Center on Ageing, HKU
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing eCoaching for Caregivers of Older Adults and eCoaching (need specific) for Caregivers of Older Adults in people with Caregiver Burden and Self Efficacy, run by The University of Hong Kong at 1 site in Hong Kong.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 6 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 10 Jun 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Hong Kong. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Vivian Lou, PhD (3917 4835, wlou@hku.hk), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Patient Health Questionnaire (PHQ-9) (time frame: 3 months). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT06604481, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 10 Jun 2025.