Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06561139

Mindfulness as an add-on Intervention in Treatment for Problem Gambling in Clinical Settings in Sweden

Led by Region Skane · Updated on 2024-08-21

60

Participants Needed

1

Research Sites

124 weeks

Total Duration

On this page

Sponsors

R

Region Skane

Lead Sponsor

L

Lund University

Collaborating Sponsor

AI-Summary

What this Trial Is About

This study will test the effects of an add-on mindfulness intervention for patients with gambling problems, added to treatment as usual, compared to a waitlist control condition. The study will primarily aim to decrease gambling behaviour compared to the control condition which receives the intervention later, after two months, and secondarily to decrease symptoms of depressive and anxiety symptoms. In addition, patients who have undergone the mindfulness intervention will be offered participation in a qualitative interview study aiming to deepen the understanding of feasibility and challenges of a mindfulness add-on intervention against gambling problems.

CONDITIONS

Official Title

Mindfulness as an add-on Intervention in Treatment for Problem Gambling in Clinical Settings in Sweden

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Enrolled in any kind of treatment for problem gambling at a regional health care unit for problem gambling or at any municipal social service unit for problem gambling, and who provides informed consent
Not Eligible

You will not qualify if you...

  • Inability to provide informed consent due to language difficulties or due to severe mental health problems, or because of mental health problems requiring urgent psychiatric management (such as suicidal, homicidal, delirious or psychotic behavior)

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

Malmö Addiction Center

Malmö, Sweden

Actively Recruiting

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Research Team

A

Anders Håkansson, PhD

CONTACT

P

Patrick Bacquin, nurse

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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