Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT05927987

Feasibility and Acceptability of Problem Management Plus (PM+) for Prisoners in the Netherlands - a Pilot RCT

Led by VU University of Amsterdam · Updated on 2024-12-05

60

Participants Needed

1

Research Sites

80 weeks

Total Duration

On this page

Sponsors

V

VU University of Amsterdam

Lead Sponsor

N

Netherlands Institute for the Study of Crime and Law Enforcement (NSCR)

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this pilot randomised controlled trial is to evaluate the feasibility and acceptability of the - specifically to the prison context adapted - World Health Organization's Problem Management Plus (PM+) intervention for individuals detained in Dutch remand prisons. The main question\[s\] it aims to answer are: * To what extent is the contextually adapted PM+ intervention feasible and acceptable for individuals detained in Dutch remand prisons? * To what extent are there preliminary indications of pre to post-effects of the PM+ intervention on, for example, anxiety and depression symptoms? Researchers will compare two groups to answer these questions. Participants will either receive the PM+ intervention and Care-as-Usual or only Care-as-Usual.

CONDITIONS

Official Title

Feasibility and Acceptability of Problem Management Plus (PM+) for Prisoners in the Netherlands - a Pilot RCT

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • 18 years old or above
  • Imprisoned in a Dutch prison
  • Held on remand
  • Dutch-speaking
  • Elevated levels of psychological distress (K10 >15)
Not Eligible

You will not qualify if you...

  • Enclosed in a penitentiary psychiatric centre
  • Presents a potential security risk to the research team
  • Acute medical condition
  • Imminent suicide risk or acute protection needs
  • Severe mental disorder (psychotic disorders, substance dependence)
  • Severe cognitive impairment (e.g., intellectual disability or dementia)
  • Currently enrolled in a specialized psychological treatment program (e.g., EMDR, CBT)
  • Less than two months on a stable dose of psychotropic medication (if applicable)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Vrije Universiteit Amsterdam

Amsterdam, Netherlands

Actively Recruiting

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Research Team

M

Mathilde JF van Oudenaren, MSc

CONTACT

A

Anke B Witteveen, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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