Comparing the effectiveness of two online interventions for sub-threshold and mild obsessive-compulsive symptoms: a randomised controlled trial

Not Applicable

Recruiting

• Conditions: Obsessive-compulsive symptoms; Depressive symptoms; Anxiety symptoms; Mental Health - Anxiety; Mental Health - Depression; Mental Health - Other mental health disorders

• Registration Number: ACTRN12621000419864
• Lead Sponsor: Monash University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2021-04-15
• Last Update Posted: 4 April 2022

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 100

Inclusion Criteria

Participants will a) endorse sub-clinical or mild obsessive-compulsive symptoms, as define by Dimensional Obsessive-Compulsive Scale (DOCS) scores >11 and <32, and b) be fluent in English.

Exclusion Criteria

The following exclusion criteria will be used to screen out severe presentations that potentially need more intensive or disorder-specific interventions, or to control for confounding impact of parallel treatment changes: (a) a history of psychotic symptoms (b) acute suicidal tendencies, (c) or have begun or modified psychiatric or psychological treatment within 8 weeks of beginning the study,

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Change in psychological flexibility sub scores, as measured by the Multidimensional Psychological Flexibility Inventory[6 weeks after baseline (primary timepoint). Follow-up timepoint changed to 18 weeks after baseline. ];Change in psychological inflexibility sub scores, as measured by the Multidimensional Psychological Flexibility Inventory[6 weeks after baseline (primary timepoints). Follow-up timepoint changed to 18 weeks after baseline. ];Change in obsessive-compulsive symptoms, as measured by the Dimensional Obsessive-Compulsive Scale[6 weeks after baseline (primary timepoints). Follow-up timepoint changed to 18 weeks after baseline. ]