- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01381250
Effects of Internet-based Treatment of Pathological Gambling
June 29, 2011 updated by: Umeå University
Prediction and Treatment Outcome of Internet-based Treatment of Pathological Gambling With Three-year Follow-up
A trial testing the outcome of an Internet-based treatment of pathological gambling with the hypothesis that there will be improvements both immediately and up to 36 months.
It is also hypnotized that treatment response can be predicted from background variables.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
284
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Umea, Sweden
- University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Pathological gambling according to DSM and having gambled at least once the past month
- Being atleast 18 years old
- Living in Sweden
Exclusion Criteria:
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Treatment
The treatment was based on established cognitive behavior therapy methods, as described in self-help books (Hodgins, 2002; Ladouceur & Lachance, 2006).
The text was divided into eight modules and was adapted for Internet use.
The first four modules had a motivational interviewing focus and included building motivation for change by letting the participant answer open-ended questions that would evoke talk of change.
The participants were encouraged to ask for input from their relatives on different aspects of their gambling.
In addition, the first four modules included time line follow-back and mapping of the reasons for gambling.
The remaining four modules were based on CBT.
Each module included information and exercises and ended with three to eight essay-style questions.
Feedback on homework assignments was usually given within 24 hr after participants had sent their answers via e-mail.
Once weekly, a telephone call was made by the therapists to each participant.
|
The treatment was based on established cognitive behavior therapy methods, as described in self-help books (Hodgins, 2002; Ladouceur & Lachance, 2006).
The text was divided into eight modules and was adapted for Internet use.
The first four modules had a motivational interviewing focus and included building motivation for change by letting the participant answer open-ended questions that would evoke talk of change.
The participants were encouraged to ask for input from their relatives on different aspects of their gambling.
In addition, the first four modules included time line follow-back and mapping of the reasons for gambling.
The remaining four modules were based on CBT.
Each module included information and exercises and ended with three to eight essay-style questions.
Feedback on homework assignments was usually given within 24 hr after participants had sent their answers via e-mail.
Once weekly, a telephone call was made by the therapists to each participant.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
The National Opinion Research Center DSM Screen for Gambling Problems (NODS)
Time Frame: 1 month
|
1 month
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Hospital Anxiety and Depression Scale
Time Frame: 1 week
|
1 week
|
Quality of Life Inventory
Time Frame: Present moment
|
Present moment
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Per Carlbring, PhD, Umea University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
May 1, 2004
Primary Completion (Actual)
January 1, 2006
Study Completion (Actual)
January 1, 2009
Study Registration Dates
First Submitted
June 22, 2011
First Submitted That Met QC Criteria
June 23, 2011
First Posted (Estimate)
June 27, 2011
Study Record Updates
Last Update Posted (Estimate)
June 30, 2011
Last Update Submitted That Met QC Criteria
June 29, 2011
Last Verified
January 1, 2004
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- Spelstudie2
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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