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Internet Delivered CBT for Olfactory Reference Syndrome

NCT ID: NCT03846076

Last Updated: 2021-11-02

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

15 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-03-04

Study Completion Date

2021-04-12

Brief Summary

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The primary aim of the study is to test the feasibility and efficacy of, a manual based, Internet-delivered, cognitive behaviour therapy (CBT) for patients with Olfactory Reference Syndrome (ORS) who live in Sweden. The secondary aim is to investigate smell sensitivity and body odor in these ORS-patients.

Detailed Description

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Conditions

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Olfactory Reference Syndrome

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Internet-delivered CBT

10 weeks of CBT delivered via the Internet.

Group Type EXPERIMENTAL

Cognitive behavioral therapy

Intervention Type BEHAVIORAL

Cognitive behavioral therapy

Interventions

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Cognitive behavioral therapy

Cognitive behavioral therapy

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Primary diagnosis of ORS
* Outpatients
* Male or female
* Signed informed consent
* Have regular access to a computer with Internet access and skills to use the web

Exclusion Criteria

* Not able to read or understand the basics of the ICBT self-help material
* Psychotropic medication changes within two months prior to treatment
* Completed CBT for ORS within last 12 months
* Ongoing substance dependence or misuse
* Lifetime bipolar disorder or psychosis
* Suicidal ideation
* Axis II diagnosis that could jeopardize treatment participation
* Serious physical illness that will be an obstacle in ICBT
* Other ongoing psychological treatments that could affect ORS symptoms
* Epilepsia
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Region Stockholm

OTHER_GOV

Sponsor Role collaborator

Volen Ivanov

OTHER

Sponsor Role lead

Responsible Party

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Volen Ivanov

Principal Investigator

Responsibility Role SPONSOR_INVESTIGATOR

Locations

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M46: Karolinska Universitetssjukhuset, Psykiatri Sydväst Stockholm, Huddinge, Sweden, 141 86

Stockholm, , Sweden

Site Status

Countries

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Sweden

Other Identifiers

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2019-00775

Identifier Type: -

Identifier Source: org_study_id