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RECRUITING
NCT07362511
NA

Imagery Rescripting in Primary Care

Sponsor: University of Amsterdam

View on ClinicalTrials.gov

Summary

In the current study we aim to investigate the feasibility, acceptability, and effectiveness of ImRs offered by mental health assistants within primary care to reduce depressive symptoms. In a single-case experimental design (SCED) study, the following hypotheses will be tested: 1. ImRs results in a reduction of depressive symptoms compared to baseline, and this reduction lasts up to six months. 2. Patients with complaints of depressive symptoms find ImRs an acceptable form of intervention when offered by mental health assistants within a general practice setting. Participants will wait for 2-4 weeks and then receive 5 sessions of ImRs over a period of 10 weeks. During these sessions, negative memories related to their depressed feelings are rescripted.

Official title: Imagery Rescripting Within Primary Care to Manage Depression: A Single-Case Experimental Design

Key Details

Gender

All

Age Range

18 Years - 70 Years

Study Type

INTERVENTIONAL

Enrollment

12

Start Date

2025-12-01

Completion Date

2027-01-31

Last Updated

2026-01-23

Healthy Volunteers

No

Interventions

BEHAVIORAL

Imagery Rescripting

During ImRs, the patient brings a negative memory to mind and changes, together with the therapist, the outcome of the memory into a more positive

Locations (1)

UvA Huisartsen

Amsterdam, North Holland, Netherlands