EmRT: Computerized Training for Individuals Diagnosed With Obsessive-Compulsive and Related Disorders

Sponsor
Stanford University (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT03182075
Collaborator
(none)
40
1
2
77.1
0.5

Study Details

Study Description

Brief Summary

Obsessive-Compulsive Disorder (OCD) is a chronic and disabling disorder that costs the economy over $2 billion annually and represents a significant public health problem. This study aims to build on our understanding of aberrant emotional processing in OCD. The proposed project tests whether a computerized training aimed to alter emotional processes, can relieve repetitive thoughts and behaviors.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Computerized Training
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
40 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Supportive Care
Official Title:
Emotional Reactivity Training for Obsessive-Compulsive and Related Disorders
Actual Study Start Date :
Apr 30, 2018
Anticipated Primary Completion Date :
Jul 1, 2024
Anticipated Study Completion Date :
Oct 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Active Training

OCD participants will receive active emotional reactivity training (14 sessions) via computer.

Behavioral: Computerized Training
OCD participants will receive 14 sessions of training via computer within 3 weeks.

Sham Comparator: Passive Training

OCD participants will receive passive computerized training (14 sessions) via computer.

Behavioral: Computerized Training
OCD participants will receive 14 sessions of training via computer within 3 weeks.

Outcome Measures

Primary Outcome Measures

  1. Yale-Brown Obsessive Compulsive Scale (for participants diagnosed with OCD) [up to 2 months]

    Improvement in OCD severity is measured by the YBOCS (Yale Brown Obsessive-Compulsive Scale), a gold standard measure of obsessions and compulsions. For the YBOCS the minimum units are 0 and Maximum units on the total scale are 40. The higher the number on the YBOCS, the more severe the symptoms. Response is defined as at least a 35% reduction on the YBOCS.

  2. Savings Inventory Revised Scale (for participants diagnosed with hoarding disorder) [up to 2 months]

    The SI-R is a 23-item questionnaire with 3 factor-analytically defined sub-scales for difficulty discarding, excessive clutter, and compulsive acquisition.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • age 18 years old and older

  • primary diagnosis of OCD

  • sufficient severity of OCD symptoms

  • Stable on psychotropic or other medication

  • capacity to provide informed consent

Exclusion criteria:
  • psychiatric or medical conditions that make participation unsafe

  • concurrent use of any medications that might increase the risk of participation

  • concurrent Cognitive-Behavioral therapy for OCD

Contacts and Locations

Locations

Site City State Country Postal Code
1 Stanford University Stanford California United States 94305

Sponsors and Collaborators

  • Stanford University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

None provided.
Responsible Party:
Carolyn Rodriguez, Assistant Professor, Stanford University
ClinicalTrials.gov Identifier:
NCT03182075
Other Study ID Numbers:
  • 40185
First Posted:
Jun 9, 2017
Last Update Posted:
Jun 21, 2022
Last Verified:
Jun 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Carolyn Rodriguez, Assistant Professor, Stanford University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 21, 2022