Clinical Trial

Imagery Rescripting in Primary Care

Study acronym: IMPACT MADE
Recruiting
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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.
Trial Details
NCT Number NCT07362511
Lead Sponsor University of Amsterdam
Collaborators: UvA Huisartsen
Conditions Major Depressive Diorder, Low Self-Esteem, Mood Disorders
Enrollment 12 participants
Start Date 2025-12-01
Primary Completion 2026-08-31 (estimated)
Study Completion 2027-01-31 (estimated)
Updated on ClinicalTrials.gov 2026-01-23