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Clinical Trials/NCT03212703
NCT03212703CompletedNot Applicable

A Trial of Mindfulness-Based Skills Training Groups Versus a Waiting List Control Period for Parents of Obsessive-Compulsive Disorder (OCD)-Affected Youth

University of British Columbia1 site in 1 country39 target enrollmentStarted: July 1, 2015Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
39
Locations
1
Primary Endpoint
Change in parental stress levels compared to waiting list control (WLC).

Study Overview

Brief Summary

The purpose of this study is to investigate the role of a mindfulness-based skills training program for parents of children with obsessive compulsive disorder (OCD). The investigators will explore if parents involved in this group experience any change in their levels of stress, feelings of being an effective parent and family relationships compared to a waiting list control period. The investigators will look at how the family manages OCD in their lives. In particular, if mindfulness skills training will help increase the parents ability to tolerate distress in their child secondary to OCD and as such reduce the family accommodation of OCD. As family accommodation is an important negative prognostic predictor for children with OCD, changes in OCD symptom severity and functional impact in these child will also be measured.

Detailed Description

Obsessive-compulsive disorder (OCD) is a debilitating psychiatric illness that frequently begins in childhood. It is characterized by obsessions and/or compulsions that are distressing, time consuming and significantly impairing. OCD is distinct in the extent to which it disrupts family functioning, in that there is intense parental pressure to become involved in rituals and to change home environments and schedules to avoid triggers, thus accommodating the OCD. It is also well known that OCD severity tends to worsen in the context of stressful environments and situations. While effective treatment approaches for pediatric OCD have been identified, partial response and treatment refusal are all too common, leading to chronicity of both the illness itself and of its deleterious familial effects.

The investigators plan to study a novel approach to help manage the stress of parenting a child with OCD, thus facilitating more effective resistance to OCD family accommodation and supporting the child in fighting this difficult illness. The investigators will explore the role of group-based mindfulness-based skills training (P-MBST) in supporting parents of OCD-affected youth, in particular investigating the possibility that increased distress tolerance as a result of mindfulness practice may help parents reduce OCD accommodation.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Parents (or step-parents or legal guardians) with care-giving role for an OCD-affected youth from our clinic
  • •Participants must be able to converse in English
  • •Participants willing to attend 8 sessions of a weekly 1.5 hour group, in addition to complete questionnaires at multiple time points during the group and waiting list period.

Exclusion Criteria

  • •Parents who have previously participated in mindfulness skills training.
  • •Parents with active psychosis, mania, mental retardation, autism or current substance misuse.
  • •Parents unwilling to provide consent.
  • •Families who are not attending our program's group-family Cognitive-Behavioral Therapy treatment concurrently.

Arms & Interventions

Waitlist control (WLC)

Active Comparator

Observation surveys over an 8-week period.

Intervention: Mindfulness-Based Skills Training (MBST) (Behavioral)

Mindfulness-Based Skills Training (MBST)

Active Comparator

Attendance at weekly 1.5-hour group sessions and surveys over an 8-week period.

Intervention: Waitlist control (WLC) (Other)

Outcomes

Primary Outcomes

Change in parental stress levels compared to waiting list control (WLC).

Time Frame: Baseline (first week of P-MBST), Mid-treatment (fifth week of P-MBST), Post-treatment (within one week of completing 8-week P-MBST sessions) and follow-up (one month following P-MBST)

Parental stress levels is measured using the Parenting Stress Index - Short Form (PSI-SF) for parents with children under 13 years of age and the Stress Index for Parents of Adolescents - Short Form (SIPA-SF) for parents with children who are 13 years and older. The PSI-SF and SIPA-SF are both measures of parental stress, but with a difference in age cut-off.

Change in ability to tolerate OCD-related distress compared to waiting list control (WLC).

Time Frame: Baseline (first week of P-MBST), Mid-treatment (fifth week of P-MBST), Post-treatment (within one week of completing 8-week P-MBST sessions) and follow-up (one month following P-MBST)

The ability to tolerate OCD-related distress is measured using the Parental Tolerance of Child Distress (PT-OCD) scale.

Secondary Outcomes

  • Change in ability to resist family accommodation of the child's OCD symptoms compared to waiting list control (WLC).(Baseline (first week of P-MBST), and Post-treatment (within one week of completing 8-week P-MBST sessions).)
  • Change in family functioning compared to the waiting list control (WLC).(Baseline (first week of P-MBST), and Post-treatment (within one week of completing 8-week P-MBST sessions).)
  • Change in OCD-associated coercive and disruptive symptoms compared to waiting list control (WLC).(Baseline (first week of P-MBST), and Post-treatment (within one week of completing 8-week P-MBST sessions).)
  • Change in OCD severity compared to waiting list control (WLC).(Baseline (first week of P-MBST), and Post-treatment (within one week of completing 8-week P-MBST sessions).)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Evelyn Stewart, MD

Principal Investigator

University of British Columbia

Study Sites (1)

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