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What Are You Looking for? Psychometric and Experimental Analyses of Reassurance Seeking in Obsessive-compulsive Disorder

What Are You Looking for? Psychometric and Experimental Analyses of Reassurance Seeking in Obsessive-compulsive Disorder

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02909660
Enrollment
7
Registered
2016-09-21
Start date
2016-09-30
Completion date
2017-11-30
Last updated
2017-12-12

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

Conditions

Obsessive-Compulsive Disorder

Brief summary

This study evaluates the efficacy and acceptability of two cognitive-behavioural interventions for reassurance seeking behaviour in obsessive-compulsive disorder (OCD), a family accommodation reduction protocol vs. a novel support-seeking protocol. Half of participants will be randomly assigned to participate in the support-seeking intervention, whereas the other half will participate in the family accommodation reduction intervention.

Detailed description

An existing family accommodation reduction intervention to reduce reassurance seeking behaviour in OCD (which represents treatment as usual, or TAU) is being compared to a novel support-seeking intervention to determine which is more efficacious and acceptable to participants. The TAU protocol asks participants to make an agreement with their significant others to withhold reassurance when it is sought. It is believed that this behaviourally-based intervention encourages extinction of reassurance seeking over time by eliminating reinforcement of the behaviour by significant others. The support-seeking intervention asks participants to move towards adaptively seeking support from a significant other to manage anxiety or distress rather than seeking reassurance. Significant others are taught to provide support rather than reassurance. It is believed that support-seeking may reduce reassurance seeking behaviour because it helps participants manage the anxiety or distress that underlies the requests for reassurance without interfering with disconfirmatory learning.

Interventions

Empirically-supported psychological intervention for various mental health concerns including obsessive-compulsive disorder (OCD). Includes components to foster cognitive (i.e., thinking) and behavioural changes.

Sponsors

Concordia University, Montreal
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Diagnosis of OCD * Engaging in reassurance seeking more than once a day about the same thing * Willingness to allow the experimenter to contact a significant other from whom the participant seeks reassurance regularly * Ability to read, write, and communicate in English

Exclusion criteria

* Current suicidal ideation/intent * Current substance abuse * Psychosis * Diagnosis of bipolar disorder (I or II) * If participants are on medication they must be on a stable dose (i.e., have maintained a consistent dose for at least three months) and agree not to change their medication regimen for the duration of the study

Design outcomes

Primary

MeasureTime frameDescription
Three-week follow-up: Endorsement and Discomfort Scales (EDS; Tarrier, Liversidge, & Gregg, 2006)Three-week follow-upValidated questionnaire assessing acceptability of and discomfort caused by an intervention.
One-week follow-up: Endorsement and Discomfort Scales (EDS; Tarrier, Liversidge, & Gregg, 2006)One-week follow-upValidated questionnaire assessing acceptability of and discomfort caused by an intervention.
Three-week follow-up: Treatment Acceptability and Adherence Scale (TAAS; Milosevic, Levy, Alcolado, & Radomsky, 2015)Three-week follow-upValidated questionnaire assessing how acceptable participants find an intervention as well as ease of adherence.
Self-reported reassurance seeking behaviour5 weeks (baseline through 3 week follow-up)Number of times participants self-report seeking reassurance per day
Self-reported support-seeking behaviour4 weeks (condition assignment through 3 week follow-up)Number of times participants in the support-seeking condition self-report seeking reassurance per day
Self-reported anxiety5 weeks (baseline monitoring through 3 week follow-up)Level of anxiety on average per day, self-rated from 0-100
One-week follow-up: Treatment Acceptability and Adherence Scale (TAAS; Milosevic, Levy, Alcolado, & Radomsky, 2015)One-week follow-upValidated questionnaire assessing how acceptable participants find an intervention as well as ease of adherence.

Secondary

MeasureTime frameDescription
Change in anxietyBaseline (monitoring week 1) to end of reassurance provision week (monitoring week 2)Pre-post assessment of change in participants' self-reported anxiety ratings, as rated from 0-100
Change in self-reported reassurance-seekingBaseline to one-week follow-up and baseline to three-week follow-upPre-post assessment of change in the number of times per day that participants self-report reassurance seeking behaviour from the baseline monitoring week to the follow-up assessments.

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026