An interventional study of iCBT in Gambling, sponsored by Indonesia University. Not yet recruiting. Open to participants aged 18 Years to 59 Years. Per ClinicalTrials.gov, last updated 2024-07-11.
Sponsored by Indonesia University · Not applicable, Interventional, and Treatment
Gambling disorder (GD) has become a wide concern in Indonesia, as many negative consequences aroused from this psychiatric condition. Prompt treatment with appropriate method of delivery is required to achieve optimal outcome in GD patients. This study aims to determine the effectiveness and feasibility of internet-based cognitive behavioral therapy (iCBT) in treating GD.
This non-randomised pilot and feasibility study will recruit 20 people with GD. All participants will receive the iCBT intervention through self-learning videos and guided weekly group sessions. The effectiveness of the intervention will be assessed at baseline (week 0), post-treatment completion (week 10), and 6 weeks post-treatment (week 16).
Expanded access of the iCBT module will not be available until after the study completion.
158 studies on the registry are indexed under Gambling; 42 are open to participants now.
This study's planned enrollment of 20 is below the median of 66 across 128 interventional studies indexed under Gambling.
Browse Gambling studies →Indonesia University is the lead sponsor of 446 studies on the registry; 56 are open to participants now.
Of its 6 completed or terminated interventional studies of FDA-regulated products, 1 (17%) have results posted.
Counted across the registry records on this site, refreshed daily.
Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.
Exclusion Criteria:
Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Informed consent
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
10 guided therapy sessions (once-weekly) with each session lasting 20 minutes.
Behavioral: iCBT
All participants will undergo 10 guided therapy sessions (once-weekly) with each session lasting 20 minutes. The therapy module will be given as an online self-learning source via videos in a website specifically developed for this training. The videos will divide the module content into several parts with each video lasting about 10 minutes.
Gambling symptom severity
a decrease in Gambling Symptom Assessment Scale (G-SAS) score
Time frame: G-SAS will be assessed at baseline (week 0), post-treatment (week 6), and follow-up (week 16)
Problem gambling severity
a decrease in Problem Gambling Severity Index score
Time frame: PGSI will be assessed at baseline (week 0), post-treatment (week 6), and follow-up (week 16)
Gambling urges
a decrease in Gambling Urge Scale (GUS) score
Time frame: GUS will be assessed at baseline (week 0), post-treatment (week 6), and follow-up (week 16)
Gambling-related cognitive distortions
a decrease in Gambling Related Cognitions Scale (GRCS) score
Time frame: GRCS will be assessed at baseline (week 0), post-treatment (week 6), and follow-up (week 16)
Nonspecific psychological distress
a decrease in Self Rating Questionnaire-20 (SRQ-20) score
Time frame: SRQ-20 will be assessed at baseline (week 0), post-treatment (week 6), and follow-up (week 16)
Subjective quality of life
an increase in World Health Organization Quality-of-Life Scale (WHOQOL-BREF) score
Time frame: WHOQOL-BREF will be assessed at baseline (week 0), post-treatment (week 6), and follow-up (week 16)
No study locations are listed for this record.
This study is not yet recruiting, as verified in Jul 2024. You cannot join it, but the record below documents what was studied.
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