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Imagery Rescripting in Primary Care

NCT07362511 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 12

Last updated 2026-01-23

No results posted yet for this study

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.

Conditions

  • Major Depressive Diorder
  • Low Self-Esteem
  • Mood Disorders

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

Sponsors & Collaborators

  • UvA Huisartsen

    collaborator UNKNOWN

  • University of Amsterdam

    lead OTHER

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-12-01
Primary Completion
2026-08-31
Completion
2027-01-31

Countries

  • Netherlands

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07362511 on ClinicalTrials.gov