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Contingency Management as an Adjunct Treatment for Rural and Remote Disordered Gamblers

Piloting the Addition of Contingency Management to Best Practice Counselling as an Adjunct Treatment for Rural and Remote Disordered Gamblers

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02953899
Enrollment
54
Registered
2016-11-03
Start date
2016-11-01
Completion date
2026-12-31
Last updated
2026-05-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gambling Disorder

Keywords

Internet, Contingency Management, Gambling Disorder, Rural

Brief summary

The purpose of this project is to pilot contingency management as an adjunct treatment to counselling as usual using internet delivered video-conferencing applications for remote disordered gamblers. This project further investigates the impact of adding contingency management to counselling to improve counselling attendance and retention and uses internet-delivered approaches to assist rural and remote disordered gamblers gain access to counselling treatments.

Detailed description

The chosen methodology is a randomised clinical trial where participants are allocated into one of two conditions; Contingency Management and Cognitive Behavioural Therapy (CM+), or Cognitive Behavioural Therapy alone (CBT) for the treatment of disordered gambling. Participants will experience a battery of tests pre- and post-treatment examining clinical, psychological, and behavioural issues, including co-morbid substance use. Alberta Rural Development Network (ARDN) affiliates will be provided with information regarding how participants can access the Qualtrics study site (e.g., an on-line survey hosting company) and will be individually directed to the study site by the principal investigator to complete the consent form and the base-line assessments. Counselling will be provided free of charge using Skype or Facetime video-conferencing internet applications. Participation in each condition will last 14 weeks: 12 weeks for treatment, and 2 weeks of assessments (one week prior to treatment and one week post treatment). Pre-treatment assessments (including demographic information) will take approximately 30-45 minutes, as will the post-treatment assessments. The progress check-ups by the Principal Investigator will take 5 to 10 minutes. A subset of treatment seekers, counsellors, and community/project stakeholders (e.g., ARDN affiliates) will also be chosen to participate in qualitative interviews to explore their experiences as well as their perceptions regarding the utility of the program for residents of rural and remote areas. The qualitative interviews will take approximately 30-60 minutes.

Interventions

BEHAVIORALContingency Management

In addition to Cognitive Behavioural Therapy, this intervention uses small incentives to reinforce study attendance and gambling abstinence.

BEHAVIORALCognitive Behavioural Therapy

This intervention uses psychoeducation, behavioural strategies, and cognitive restructuring to assist the participant in their efforts to become abstinent from gambling.

Sponsors

University of Lethbridge
Lead SponsorOTHER
Rural Development Network
CollaboratorUNKNOWN

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

* capable of providing written consent, * received a diagnosis of gambling disorder (American Psychiatric Association, 2013), * gambled within the last month, * live in a rural or remote location, and * speak English

Exclusion criteria

* Medically unmanaged psychiatric or neurological disorder(s) except for disordered gambling

Design outcomes

Primary

MeasureTime frameDescription
Gambling Abstinence12 weeksThe total number of sessions that a participant provided evidence of gambling abstinence in the study

Secondary

MeasureTime frameDescription
Session Attendance12-weeksThe total number of sessions that a participant attended the study
Study Retention12-weeksThe total number of weeks that a participant attended the study

Countries

Canada

Contacts

CONTACTDarren R Christensen, PhD
darren.christensen@uleth.ca403-329-5124
CONTACTChad Witcher, PhD
chad.witcher@uleth.ca403-332-4439
PRINCIPAL_INVESTIGATORDarren R Christensen, PhD

University of Lethbridge

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 12, 2026