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Study identifier: NCT04071990 Synced from ClinicalTrials.gov · July 28, 2026
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Family Involvement in CBGT of OCD: a Randomized Controlled Trial

Condition: Obsessive-Compulsive Disorder  ·  Sponsor: University Hospital, Ghent

PhaseNA
Planned participants80
Who can joinAll sexes, 18 Years to 65 Years
Healthy volunteersNo

About this study

With a lifetime prevalence of 1-3% Obsessive-Compulsive Disorder (OCD) is a chronic and disabling psychiatric disorder with considerable burden for the individual and society. Cognitive-behavioural group therapy (CBGT) is effective in reducing the intensity of OCD symptoms and it improves the OCD patient's quality of life. There is also growing evidence that family accommodation (FA) maintains and/or facilitates OCD symptoms, reinforces fear and avoidance behaviours in patients with OCD and is associated with family burden. Considering the promising results of involvement of family in CBGT on OCD symptoms and FA, the current study aims at investigating the effects of the involvement of the family in a 12-week CBGT protocol on the OCD symptoms, FA, burden, QOL, anxiety and depressive symptoms in OCD patients and their live-in relatives. Eighty patients with OCD and their live-in family members (partner, parent, sibling, …) between 18-65 years old will be included in this randomized controlled trial. Patients and family members will be randomly assigned to CBGT with the involvement of family or to CBGT without involvement of family. The primary goal of this study is to evaluate the effects of the involvement of live-in family members during a 12-week CBGT on OCD symptomatology and family accommodation during a 12-month follow-up period. In a secondary stage, we will explore whether the involvement of live-in family members during a 12-week CBGT will ameliorate anxiety and depre…

This description comes directly from the study's public registry record.

Talk to the study team

Hannelore LN Tandt, MD  ·  +3293324394  ·  hannelore.tandt@uzgent.be

Gilbert MD Lemmens, MD, PhD  ·  +3293324394  ·  gilbert.lemmens@uzgent.be

Always discuss trial participation with your own doctor first.

Locations (1)

Ghent University HospitalGhent, BelgiumRecruiting

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Source record: clinicaltrials.gov/study/NCT04071990