Imagery Rescripting in Primary Care
Recruiting
N/A
Interventional Study
Major Depressive Diorder
Low Self-Esteem
Mood Disorders
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 70
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 12 (estimated)
- Sponsor
- University of Amsterdam · Other
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About This Trial
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.
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Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Main complaint of depressive feelings, as indicated by both the mental health assistant and the patient.
* HADS score for the depression subscale ≥ 11.
* Ability to understand, read, write and speak Dutch or English.
* Age between 18 and 70.
* Willingness to participate in the…
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