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Development and evaluation of a pain management training program for dementia caregivers based on the ADDIE model

Development and evaluation of a pain management training program for dementia caregivers based on the ADDIE model

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500105191
Enrollment
Unknown
Registered
2025-06-30
Start date
2025-07-01
Completion date
Unknown
Last updated
2025-07-07

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

Conditions

Dementia

Interventions

Interventional group:Pain management training was provided to caregivers of patients with dementia in the intervention group for about four weeks
Control group:Caregivers in the control group will receive a pain management manual at the same time as the caregivers in the intervention group before the start of the training and will not receive a

Sponsors

Nanjing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. The patient under care must meet the following prerequisites: hospital-diagnosed dementia, including Alzheimer's disease and other types of dementia; 2. Formal personnel who undertake the main care of dementia patients, that is, medical nurses working in hospitals, nursing institutions, rehabilitation centers, etc., with a care duration of > = 1 month; 3. The dementia patient under care has diseases that cause pain signs (such as neurogenic pain, musculoskeletal diseases, gastrointestinal diseases, physical injuries, etc.); 4. Be conscious, willing to participate, and be able to understand and answer questions correctly.

Exclusion criteria

Exclusion criteria: Halfway out of the researcher for various reasons.

Design outcomes

Primary

MeasureTime frame
Pain management ability;

Secondary

MeasureTime frame
Pain in patients with dementia;

Countries

China

Contacts

Public ContactDingYaping

Nanjing Medical University

dingyp@njmu.edu.cn+86 25 8686 9562

Outcome results

None listed

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