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Evaluation of Two Treatments for Chronic Post Concussion Syndrome

S

Simon Fraser University

Status and phase

Terminated
Phase 2
Phase 1

Conditions

Head Injury
Post Concussion Syndrome

Treatments

Behavioral: Relaxation Training
Behavioral: Interoceptive Exposure
Behavioral: Psychoeducation

Study type

Interventional

Funder types

Other

Identifiers

NCT00871884
1234567

Details and patient eligibility

About

This study is designed to investigate factors that are associated with prolonged recovery from mild head injury. The investigators are particularly interested in defining the impact of anxiety related variables, such as health anxiety and anxiety sensitivity in the maintenance of symptoms.

A further goal of the study is the evaluation of two treatment methods that have been proposed to be effective in reducing the impact of post concussion symptoms. The investigators hypothesize that a treatment which is directly focused on changing these anxiety related variables will be more effective than one that does not.

Enrollment

10 patients

Sex

All

Ages

19 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Mild Head Injury at least 3 months prior to treatment
  • age 19 to 65 years
  • grade 12 education
  • proficiency with English language

Exclusion criteria

  • Current Litigation

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

10 participants in 2 patient groups

Treatment As Usual
Active Comparator group
Treatment:
Behavioral: Psychoeducation
Behavioral: Relaxation Training
Experimental
Experimental group
Treatment:
Behavioral: Psychoeducation
Behavioral: Interoceptive Exposure
Behavioral: Relaxation Training

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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