The Young Ambassadors Supporting Caregivers Program
YASC
The Effect of the Young Ambassadors Supporting Caregivers (YASC) Program: A Dual Randomized Controlled Trial
1 other identifier
interventional
120
0 countries
N/A
Brief Summary
This RCT will provide preliminary evidence on effective training for young adult volunteers to support older adult caregivers, addressing Hong Kong's aging crisis and caregiver burden. The objectives of this study include:
- 1.To examine the feasibility and acceptability of the interventions in Hong Kong's cultural context.
- 2.To evaluate the effects of three trainings (mindfulness/compassion, caregiving skills, communication skills) on young adult volunteers' preparedness for caregiving, meaning of life, and civic engagement.
- 3.To assess the impact of volunteer services on caregivers' depression, anxiety, and caregiver burden.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Oct 2025
Shorter than P25 for not_applicable
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
August 5, 2025
CompletedFirst Posted
Study publicly available on registry
August 12, 2025
CompletedStudy Start
First participant enrolled
October 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 30, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
June 30, 2026
August 12, 2025
August 1, 2025
9 months
August 5, 2025
August 5, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Preparedness for Caregiving Scale
Preparedness for Caregiving Scale will be adopted to evaluate university student volunteers' self-perceived readiness to provide care across eight critical domains, including physical/emotional caregiving (e.g., "How well prepared are you to care for emotional needs?"), stress management, and emergency response. Each item is rated on a 5-point Likert scale (0=Not at all prepared to 4=Very well prepared), providing a quantitative measure of skill development through the intervention. Higher score indicate higher level of preparedness for caregiving skills. Total score ranged from 0 to 32.
Baseline (pre-test), immediately post-test
Patient Health Questionnaire
This scale will be applied to caregivers of older adults who joined this study. The Patient Health Questionnaire (PHQ) is a widely used, self-administered screening instrument designed to facilitate the identification and assessment of common mental health disorders in clinical and research settings. Developed as part of the Primary Care Evaluation of Mental Disorders (PRIME-MD) project, the PHQ consists of several modules, each corresponding to specific psychiatric diagnoses according to DSM criteria. The most commonly used version, the PHQ-9, consists of nine items that assess the frequency of depressive symptoms over the past two weeks. Each item is scored on a four-point Likert scale (ranging from 0 = "not at all" to 3 = "nearly every day"), resulting in a total score ranging from 0 to 27. Higher scores indicate greater severity of depressive symptoms. The PHQ has demonstrated strong reliability and validity across diverse populations and is valued for its brevity, ease of use, an
Baseline (pre-test), immediately post-test
Secondary Outcomes (4)
Civic Engagement Scale
Baseline (pre-test), immediately post-test
Meaning in Life Scale
Baseline (pre-test), immediately post-test
Generalized Anxiety Disorder scale
Baseline (pre-test), immediately post-test
Zarit Burden Interview
Baseline (pre-test), immediately post-test
Study Arms (3)
Intervention: Mindfulness and Compassion Training
EXPERIMENTALStudents randomly assigned to this group will receive 12 hours over 6 weeks (2-hour weekly sessions) teaching mindfulness meditation (e.g., loving-kindness, body scan) and compassion practices (e.g., self-compassion exercises). Content culturally adapted with Buddhist-influenced terminology and practices resonant with Hong Kong's context. Caregivers assigned to this group will receive students' help based on the mindfulness training.
Intervention: Caregiving Skills Training
EXPERIMENTALStudents randomly assigned to this group will receive 12 hours over 6 weeks (2-hour weekly sessions) teaching including: Occupational therapist training (e.g., daily living support), Physical therapist training (e.g., safe transfers), Speech Therapist training (e.g., communication aids), and Registered Nurse training (e.g., vital signs monitoring), tailored to caregivers' needs. Caregivers assigned to this group will receive students' help based on the caregiver skills training.
Control: Communication Skills Training
ACTIVE COMPARATORStudents randomly assiged to this group will receive 12 hours over 6 weeks (2-hour weekly sessions) focusing on active listening, empathy, and basic conversational skills, without specific mindfulness or caregiving techniques. Caregivers assigned to this group will receive students' help based on the communication skills training.
Interventions
Parallel randomized controlled trial
Parallel randomized controlled trial
Parallel randomized controlled trial
Eligibility Criteria
Contact the study team to discuss eligibility requirements. They can help determine if this study is right for you.
Sponsors & Collaborators
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- INVESTIGATOR, OUTCOMES ASSESSOR
- Masking Details
- Due to the nature of this trial, neither the staff, university students and caregivers can be masked to allocation. The investigator data analyst will be blinded after study completion by having the intervention group information coded.
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Research Assistant Professor
Study Record Dates
First Submitted
August 5, 2025
First Posted
August 12, 2025
Study Start
October 1, 2025
Primary Completion (Estimated)
June 30, 2026
Study Completion (Estimated)
June 30, 2026
Last Updated
August 12, 2025
Record last verified: 2025-08