Skip to content

Developing and testing a brief mindfulness just-in-time adaptive intervention for reducing stress of dementia caregivers

Developing and testing a brief mindfulness just-in-time adaptive intervention for reducing stress of dementia caregivers

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300071361
Enrollment
Unknown
Registered
2023-05-12
Start date
2024-09-01
Completion date
Unknown
Last updated
2025-11-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dementia

Interventions

Phase 1 - State of Receptivity:4 days (D1-D4): Psycho-education 16 days (D5-D20): 0 to 6 ecological momentary assessment will be sent to participants
participants will be randomized into receiving mindfulness intervention or not
Phase 2 - State of Receptivity:4 days (D1-D4): Psycho-education 7 days (D5-D12): Control or Static model 7 days (D13-D20): Static, Adaptive, or Control model
Phase 3 - State of Vulnerability:4 days (D1-D4): Psycho-education
16 days (D5-D20): 0 to 6 ecological momentary assessment will be sent to participants.

Sponsors

Research Fund Secretariat, Research Office Health Bureau
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: The inclusion criteria for family dementia caregivers are: 1. Aged 18 years above; 2. Family caregiver of an individual with a confirmed medical diagnosis of any type of dementia who has been residing in the community; 3. Having been providing care for ADLs and IADLs for at least 20 hours per week for at least one year prior to recruitment; 4. Have a smartphone and 5. Have mild to moderate stress (the 14-item Chinese version Perceived Stress Scale).

Exclusion criteria

Exclusion criteria: 1. Having participated in any structured mind-body intervention, cognitive therapy, or structured psychosocial intervention in the 6 months prior to recruitment; 2. Having acute psychiatric and medical comorbidities that are potentially life-threatening (e.g. suicidal ideation) or that limit the caregivers participation or adherence (e.g. acute psychosis).

Design outcomes

Primary

MeasureTime frame
Perceived Stress;

Secondary

MeasureTime frame
Depressive Symptoms;Burden;Positive Aspect of Caregiving;Sleep Quality;Quality of Life;Mindfulness;

Countries

China

Contacts

Public ContactProf CHOU Kee Lee

The Education University of Hong Kong

klchou@eduhk.hk+852 2948 7473

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026