Clinical trial · Interventional
Care Planning for a Loved One With Dementia: Knowledge, Preparing for Decisions, and Emotions
NCT05165186CI-TRIAL-00070621unknownN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
The overall objective of this study is to compare knowledge, decisional conflict, preferences, and caregiver burden over time caregivers of Alzheimer's Disease and Related Dementias (ADRD) patients by comparing the effectiveness of a video decision aid intervention and enhanced usual care.
Conditions
Conditions (8)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Caregiver Burnout | — | UNRESOLVED | — |
| Caregiver Stress Syndrome | — | UNRESOLVED | — |
| Dementia | — | UNRESOLVED | — |
| Dementia Alzheimers | — | UNRESOLVED | — |
| Dementia Frontotemporal | — | UNRESOLVED | — |
| Dementia, Mild | — | UNRESOLVED | — |
| Dementia Moderate | — | UNRESOLVED | — |
| Dementia Severe | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Video Intervention Arm | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Video Intervention Arm
- description
- For participants randomized to the video intervention arm, participants will be shown two videos about Advanced Care Planning, and then they will be asked questions regarding the usefulness of the video and their comfort with the video
- interventionNames
- Other: Video Intervention Arm
- type
- NO_INTERVENTION
- label
- Control Arm
- description
- For participants randomized to the control group arm, participants will review an informational sheet, which covers the same information as the videos shown to the intervention arm.
Primary outcomes (3)
- measure
- Change from Baseline in percent correct and in response confidence on Knowledge of Advanced Dementia Questionnaire.
- timeFrame
- Baseline and immediately post-intervention
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * All participants must be age 18 or older. * Participants must be able to speak and understand English. * Participants must be a caregiver of someone with Alzheimer's Disease, frontotemporal dementia, or a related dementia * Participants should be able to understand the purpose and risks of the study and provide signed and dated informed consent and authorization to use protected health information (PHI) in accordance with national and local participant privacy regulations. Exclusion Criteria: \* Participants who are not able to tolerate or perform the procedures or assessments.
References
Publications (0)
Data not yet available
No reference posted for this study.