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Treatment Study for Problematic Gaming and Gambling

R

Region Skane

Status

Completed

Conditions

Internet Gaming Disorder
Pathological Gambling

Treatments

Behavioral: Treatment as usual
Behavioral: Relaps Preventions Therapy

Study type

Interventional

Funder types

Other

Identifiers

NCT05506384
2019-04797

Details and patient eligibility

About

The aim of the study is twofold: 1) to evaluate an Relaps Prevention(RP) treatment for Problematic Gaming (PG) and Internet Gaming Disorder (IGD) patients recruited from child and youth psychiatry (CAP) clinics and 2) to test whether the quality of parent-child relationships plays role in the effect of RP treatment and vice versa - whether the RP treatment has a spillover effect on the quality of parent-child relationships.

Full description

This study is a two-arm, parallel-group, single-blind, early-stage Randomized Clinical Trial (RCT) with embedded qualitative components. Participants will be randomized in a 1:1 ratio to either intervention or control, with a total of 162 participants (81+81) in the trial. The primary outcomes are measures of gaming and gambling behavior pre- and post-intervention, and the secondary outcomes include child ratings of parent-child communication, including parental knowledge, control and solicitousness about child gaming, as well as child disclosure and secrecy related to gaming.

Preliminary analyses will be conducted with regression analyses, paired sample t-tests and ANOVAs and performed in Mplus. In addition to the RCT, the study will be supplemented with a qualitative component with semi-structured individual interviews to capture participants' and clinicians' experiences of the treatment, as well as attitudes about parent-child relationships and parenting needs in carers whose children completed the RP treatment. The qualitative data will be analyzed with thematic analysis.

Enrollment

160 patients

Sex

All

Ages

12 to 18 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion criteria

  • age 12-18
  • over cut-off on GASA
  • over cut-off on CLiP

Exclusion criteria

  • not being able to speak Swedish

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

160 participants in 2 patient groups

Relaps prevention treatment
Experimental group
Description:
The treatment will be administered in an individual format and consist of seven to nine sessions of 45 minutes over a period of seven to nine weeks. The number of sessions can vary to be able to accommodate the fact that participants may have different levels of motivation for changing their primary problem behavior, which is why some participants may require one or two extra sessions at the start of the treatment. The treatment will be offered to participants both in person and via video link to facilitate participation for children and adolescents living further away from the participating clinics.
Treatment:
Behavioral: Relaps Preventions Therapy
Treatment as usual
Other group
Description:
The patients in this arm will get treatment as usual at their Child and Adolescent psychiatry clinic.
Treatment:
Behavioral: Treatment as usual

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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