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NCT03850613
Alleviating Caregivers' Stress Through an E-painting Mobile Application
NA trial testing E-painting mobile app in Caregivers in 32 participants. Completed in 30 April 2021.
30 April 2021
Quick facts
| Lead sponsor | The Hong Kong Polytechnic University |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | supportive care |
| Enrollment | 32 |
| Start date | 1 February 2018 |
| Primary completion | 30 April 2021 |
| Estimated completion | 30 April 2021 |
| Sites | 1 location across Hong Kong |
Drugs / interventions tested
- E-painting mobile app
Conditions studied
- Caregivers — all drugs for Caregivers →
- Anxiety — all drugs for Anxiety →
Sponsor
The Hong Kong Polytechnic University
Who can join
Adults 18 to 80, any sex, with Caregivers or Anxiety. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
This study aims to develop a mobile app for caregivers and tests its feasibility for a period of 8 weeks. A mixed-method study design with both qualitative and quantitative components will be used. A maximum of 36 caregivers will be involved in the six focus groups. Each focus group interview will involve 6 caregivers of persons with dementia. Another 30 caregivers will be involved in the 8-week trial use of the app. Each focus group interview will last for about 1.5 hours, facilitated by a moderator. Before and after the 8-week trial use of the app, four outcome measures (Zarit Burden Interview, Self-rated Health, Patient Health Questionnaire, and Modified Medical Outcome Study Social Support Survey) will be taken. This study will provide evidence of the feasibility of the use of the newly developed app among caregivers.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
The Use of an Electronic Painting Platform by Family Caregivers of Persons with Dementia: A Feasibility and Acceptability Study.
Leung AYM, Cheung T, Fong TKH, Zhao IY, et al · · 2022 · cited 3× · PMID 35628007 · DOI 10.3390/healthcare10050870
Verify or expand the search:
- PubMed search for NCT03850613
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Other The Hong Kong Polytechnic University trials
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT03850613 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by The Hong Kong Polytechnic University
- Last refreshed: 1 April 2025
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03850613.
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