Cognitive Behavior Therapy for Anxiety-related Asthma in Adults.

NCT ID: NCT03158194

Last Updated: 2018-03-08

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

6 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-08-16

Study Completion Date

2018-03-07

Brief Summary

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This is a study to develop a protocol on Cognitive behavior therapy (CBT) for asthma-related anxiety that in a consecutive study can be translated to internet-delivered CBT.

Detailed Description

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Asthma is one of the most common chronic diseases around the world, with a high prevalence of anxiety disorders. Cognitive behaviour therapy (CBT) has been shown to increase psychological well-being for anxiety-related asthma. Our primary aim is to develop a standardized CBT protocol for asthma-related anxiety that can be transferred to internet-delivered CBT. Ten participants will be included in a single-subject multiple baseline design. They will all receive 10-12 sessions of CBT.

Conditions

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Asthma

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Single-subject multiple baseline design.
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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CBT for anxiety-related asthma

Ten to twelve weekly sessions of CBT targeting enhanced function and decreased symptoms of anxiety.

Group Type EXPERIMENTAL

CBT for anxiety-related asthma

Intervention Type BEHAVIORAL

The specific assignments in the intervention will be based on individual behavior analysis for each participant.

Interventions

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CBT for anxiety-related asthma

The specific assignments in the intervention will be based on individual behavior analysis for each participant.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* asthma diagnosed by a physician
* anxiety or stress related to asthma

Exclusion Criteria

* severe psychiatric disorder (e.g. psychotic disorder, addiction disorder, suicidal ideation).
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Karolinska Institutet

OTHER

Sponsor Role lead

Responsible Party

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Catarina Almqvist Malmros

Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Catarina Almqvist Malmros, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Department of Medical Epidemiology and Biostatistics, Karolinska Institutet

Locations

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Department of Medical Epidemiology and Biostatistics, Karolinska Institutet

Stockholm, , Sweden

Site Status

Countries

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Sweden

Other Identifiers

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MANTRA 01

Identifier Type: -

Identifier Source: org_study_id

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