Thought Field Therapy and Cognitive Therapy for Agoraphobia

NCT ID: NCT00932919

Last Updated: 2014-04-23

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

72 participants

Study Classification

INTERVENTIONAL

Study Start Date

2006-10-31

Study Completion Date

2010-11-30

Brief Summary

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The purpose for this study is to find out if Thought field therapy has the same effect as, or better effect than, Cognitive therapy for Agoraphobia.

Detailed Description

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Thought field therapy is an alternative treatment method that has shown, by casuistic reports, to give good results when applied for anxiety disorders. In this study 72 patients will be randomized to three groups. 24 patients will receive cognitive therapy as a control method, 24 patients will receive thought field therapy. The remaining 24 patients will wait three months, and then be randomized to either of the two therapies.

Before inclusion all patients will be diagnosed with M.I.N.I. and SCID II. They will fill out self evaluation forms for symptoms and quality of life, before and after treatment, and one year after treatment.

All patients will undergo an interview with ADIS on panic and agoraphobic diagnosis and symptoms before starting treatment, and on panic and agoraphobic symptoms immediately after and one year after treatment. These interviews will be done by psychologists who are blinded for which type of treatment the patients have got.

Conditions

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Agoraphobia

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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Thought field therapy

24 randomly selected patients will be treated with 5 sessions of standard Thought field therapy.

Group Type EXPERIMENTAL

Thought field therapy

Intervention Type BEHAVIORAL

5 sessions with Thought field therapy

Cognitive therapy

Treatment with Cognitive therapy, 12 sessions with manualized therapy according to David Clark's model.

Group Type ACTIVE_COMPARATOR

Cognitive therapy

Intervention Type BEHAVIORAL

12 sessions of Cognitive therapy

Wait list

24 patients will be randomly selected to 3 months on a wait list, thereafter randomly selected to either Cognitive therapy or Thought field therapy.

Group Type OTHER

Wait list

Intervention Type BEHAVIORAL

3 months waiting, then randomized to either thought field therapy or cognitive therapy

Interventions

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Thought field therapy

5 sessions with Thought field therapy

Intervention Type BEHAVIORAL

Cognitive therapy

12 sessions of Cognitive therapy

Intervention Type BEHAVIORAL

Wait list

3 months waiting, then randomized to either thought field therapy or cognitive therapy

Intervention Type BEHAVIORAL

Other Intervention Names

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TFT CBT WL

Eligibility Criteria

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Inclusion Criteria

* Patients ages 18 years or older,
* Patients with agoraphobia,
* Patients with a score on Mobility Inventory "Alone" of 2.5 or more,
* Patients who give a written consent to participate.

Exclusion Criteria

* Psychosis (past or present),
* Drug abuse or dependency,
* Moderate or high score on suicidal behaviour on the M.I.N.I.,
* Patients who have another illness (other than panic disorder or agoraphobia) and are in need of immediate treatment.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Sorlandet Hospital HF

OTHER_GOV

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Audun C Irgens, MD

Role: PRINCIPAL_INVESTIGATOR

Sorlandet Hospital HF, Norway

Locations

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Sorlandet Hospital

Arendal, , Norway

Site Status

Countries

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Norway

References

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Irgens AC, Hoffart A, Nysaeter TE, Haaland VO, Borge FM, Pripp AH, Martinsen EW, Dammen T. Thought Field Therapy Compared to Cognitive Behavioral Therapy and Wait-List for Agoraphobia: A Randomized, Controlled Study with a 12-Month Follow-up. Front Psychol. 2017 Jun 20;8:1027. doi: 10.3389/fpsyg.2017.01027. eCollection 2017.

Reference Type DERIVED
PMID: 28676782 (View on PubMed)

Other Identifiers

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SSHF-70343-AUIR-2

Identifier Type: -

Identifier Source: org_study_id

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