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NCT03923517: RHAPSODY-plus

RHAPSODY-plus: Online Counseling for Family Caregivers of Patients With Young Onset Dementia

Completed NA Last updated 17 September 2019
What this trial tests

NA trial testing RHAPSODY online program and MEET online sessions in Early Onset Alzheimer Disease in 20 participants. Completed in 30 May 2019.

Timeline
1 January 2018
Primary endpoint
30 May 2019
30 May 2019

Quick facts

Lead sponsorTechnical University of Munich
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposeother
Enrollment20
Start date1 January 2018
Primary completion30 May 2019
Estimated completion30 May 2019
Sites1 location across Germany

Drugs / interventions tested

Conditions studied

Sponsor

Technical University of Munich

Who can join

18 and older, any sex, with Early Onset Alzheimer Disease or Frontotemporal Dementia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The RHAPSODY-plus project consists of two parts. In a first step carers of people with young onset dementia (YOD; onset before the age of 65) have the opportunity to use the RHAPSODY online program (Kurz et al., 2016) to inform themselves about different topics on young onset dementia. In a second step the participants will receive two individual counseling sessions via MEET (online videoconferencing) with a social worker and a psychologist. Goal is to investigate whether these counseling sessions have an additional benefit.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Early Onset Alzheimer Disease

Currently open trials in the same condition.

Other Technical University of Munich trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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/NCT03923517.

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