Targeting Taboo Thoughts In Obsessive-Compulsive Disorder

Sponsor
Karolinska Institutet (Other)
Overall Status
Completed
CT.gov ID
NCT04313439
Collaborator
(none)
19
1
1
16.5
1.1

Study Details

Study Description

Brief Summary

The purpose of this pilot study is to investigate if a cognitive treatment targeting obsessive beliefs in patients with aggressive obsessions is feasible and effective as an online treatment.

Condition or Disease Intervention/Treatment Phase
  • Other: Online cognitive therapy (I-CT)
N/A

Detailed Description

Patients with obsessive-compulsive disorder who presents with aggressive obsessions (also known as taboo thoughts e.g. fear of being a pedophile) and mental rituals have shown to respond less well to treatment. Thus, there is room for further innovation. The primary objective of this pilot study is to investigate if an internet-based cognitive therapy (I-CT) is feasible and effective in reducing the frequency and distress of aggressive obsessions. The study will also investigate if I-CT is associated with any significant side effects. Another objective of this study is to get a power estimate of the treatment effects for a subsequent randomized controlled study (RCT). This will be done by using an open pilot study with repeated measurements.

Study Design

Study Type:
Interventional
Actual Enrollment :
19 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Targeting Taboo Thoughts In Obsessive-Compulsive Disorder Using Internet- Delivered Cognitive Therapy
Actual Study Start Date :
Mar 26, 2020
Actual Primary Completion Date :
Feb 15, 2021
Actual Study Completion Date :
Aug 11, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: Treatment

Online Cognitive Therapy (I-CT)

Other: Online cognitive therapy (I-CT)
The treatment is an online cognitive therapy consisting of a structured self-help program over ten weeks, divided into eight modules, administered in an encrypted web platform. The program is based on the treatment manual "The treatment of Obsessions" by Stanley Rachman. In this treatment, the participant is recommended to perform daily exercises in order to identify and modify interpretations made about the importance of their obsessive thoughts. A designated therapist have email contact with the participant within the encrypted platform.

Outcome Measures

Primary Outcome Measures

  1. The clinician rated Yale Brown Obsessive Compulsive Scale (Y-BOCS) [Week 0, week 10, and 6 months follow up]

    Change in obsessions and compulsions from baseline to week 10 and 6 months after treatment has ended. Minimum value is 0. Maximum value is 40. Higher score means more symptoms.

Secondary Outcome Measures

  1. The self-rated Yale Brown Obsessive Compulsive Scale (Y-BOCS) [Weeks 0 to 10 through treatment and 6 months follow-up]

    Change in obsessions and compulsions from baseline, during treatment to week 10 and at 6 after treatment has ended. Minimum value is 0. Maximum value is 40. Higher score means more symptoms.

  2. Personal Significance Scale (PSS) [Weeks 0 to 10 through treatment and 6 months follow-up]

    Change in perceived personal significance of intrusive thougths from baseline, during treatment to week 10 and at 6 months after treatment has ended. Minimum value is 0. Maximum value is 80. Higher score means more symptoms.

  3. Montgomery Åsberg Depression Rating Scale - Self report (MADRS-S) [Week 0, week 10 and 6 months follow-up]

    Change in depression from baseline to week 10 and at 6 months after treatment has ended. Minimum value is 0. Maximum value is 40. Higher score means more symptoms.

  4. Clinical Global Impression (CGI) [Week 0, week 10 and 6 months follow-up]

    Change in symptom severity from baseline to week 10 and 6 months after treatment has ended, and treatment response and the efficacy of treatments at week 10 and 6 months after treatment after treatment has ended. Rated by the psychologist. Minimum value is 0. Maximum value is 6. Higher score means less improvement.

  5. Work and social adjustment scale (WSAS) [Week 0, week 10 and 6 months follow-up]

    Change in functional impairment from baseline to week 10 and 6 months after treatment has ended. Minimum value is 0. Maximum value is 40. Higher score means more symptoms.

  6. Thought Action Fusion Scale (TAFS) [Week 0, week 10 and 6 months follow-up]

    Change in maladaptive cognitive intrusions from baseline to week 10 and 6 months after treatment has ended. Minimum value is 0. Maximum value is 76. Higher score means more symptoms.

  7. Penn State Worry Questionnaire (PSWQ) [Week 0, week 10 and 6 months follow-up]

    Change in worry from baseline to week 10 and 6 months after treatment has ended. Minimum value is 0. Maximum value is 80. Higher score means more symptoms.

  8. Meta-Cognitive Questionnaire (Negative metacognitions subscale; MCQ-NC) [Week 0, week 10 and 6 months follow-up]

    Change in negative meta-cognitions about worrying from baseline to week 10 and 6 months after treatment has ended. Minimum value is 0. Maximum value is 24. Higher score means more symptoms.

  9. Patient Satisfaction Questionnaire (PSQ) [Week 10]

    Satisfaction of treatment at week 10. Qualitative questions.

  10. Adverse events (AE) [Weeks 0 to 10 through treatment and 6 months follow-up]

    Number of adverse events every week during treatment and post treatment week 10.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Diagnosis of OCD taboo thoughts as specified in the DSM-5

  • ≥ 18 years

  • Situated in Sweden

  • Informed consent

Exclusion Criteria:
  • No signed consent

  • Not fluent speaking in Swedish or cognitive abilities to read written material in the study

  • Adjusted pharmacological treatment the last month symptoms that may affect OCD symptoms

  • Substance dependence during the last six months

  • Psychosis

  • Ongoing mania or hypomania

  • Suicidal risk that may affect study participation

  • Personality disorder that may significantly affect the treatment participation

  • Other ongoing psychological treatments that may affect OCD-symptoms

  • Other primary psychiatric diagnosis

Contacts and Locations

Locations

Site City State Country Postal Code
1 Karolinska Institutet Stockholm Sweden 17177

Sponsors and Collaborators

  • Karolinska Institutet

Investigators

  • Principal Investigator: Erik Andersson, PhD, Karolinska Institutet

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Erik Andersson, Principal investigator, Karolinska Institutet
ClinicalTrials.gov Identifier:
NCT04313439
Other Study ID Numbers:
  • EPN Dnr 2019-06047
First Posted:
Mar 18, 2020
Last Update Posted:
Aug 17, 2021
Last Verified:
Aug 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Erik Andersson, Principal investigator, Karolinska Institutet
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 17, 2021