Internet CBT for Trichotillomania and Skin Picking Disorder

NCT ID: NCT04559750

Last Updated: 2022-09-07

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

25 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-10-05

Study Completion Date

2021-12-23

Brief Summary

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The primary aim of the study is to test the feasibility, safety and efficacy of a manual based, Internet-delivered, behavior therapy (I-BT) for trichotillomania and skin picking disorder.

Detailed Description

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Conditions

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Trichotillomania Excoriation (Skin-Picking) Disorder

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 behavior therapy (I-BT

10 weeks of (I-BT) delivered via the Internet.

Group Type EXPERIMENTAL

Internet delivered behavior therapy (I-BT)

Intervention Type BEHAVIORAL

10 weeks of I-BT

Interventions

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Internet delivered behavior therapy (I-BT)

10 weeks of I-BT

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Primary diagnosis of trichotillomania and/or skin picking disorder according to DSM-5
* Living in Sweden with a Swedish personal identification number
* Able to participate in study assessment in Swedish and understand Swedish text
* Have regular access to a computer with Internet access and skills to use Internet
* Signed informed consent
* Outpatient

Exclusion Criteria

* Psychotropic medication changes that can affect symptoms of trichotillomania or skin picking disorder within 2 months prior to treatment
* Other ongoing psychological treatments that could affect symptoms of trichotillomania or skin picking disorder
* Completed CBT for trichotillomania or skin picking disorder within the last 24 months
* Ongoing substance dependence or misuse
* Lifetime bipolar disorder or psychosis
* Suicidal ideation (a score of 5 points or higher on item 9 on the self-reported Montgomery-Åsberg depression rating scale
* Psychiatric comorbidity that could severely jeopardize treatment participation
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Region Stockholm

OTHER_GOV

Sponsor Role collaborator

Karolinska Institutet

OTHER

Sponsor Role lead

Responsible Party

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Volen Ivanov

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Psykiatri Nordväst, Stockholms Läns Sjukvårdsområde (SLSO), Region Stockholm

Stockholm, , Sweden

Site Status

Countries

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Sweden

Other Identifiers

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2019-06325

Identifier Type: -

Identifier Source: org_study_id

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