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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01327690
Other study ID # SMI-GROUP-12/10/10
Secondary ID
Status Recruiting
Phase Early Phase 1
First received
Last updated
Start date December 2010
Est. completion date December 2027

Study information

Verified date April 2024
Source Soul Medicine Institute
Contact Dawson Church
Phone 707 237 6951
Email dawsonchurch@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

PTSD (posttraumatic stress disorder) and associated mental health conditions affect both veterans and their family members. This study investigates whether group therapy using EFT (Emotional Freedom Techniques) and CBT (Cognitive Behavior Therapy) produce reductions in PTSD and comorbid symptoms.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date December 2027
Est. primary completion date December 2027
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - The ability to follow instructions, complete written forms, and provide informed consent. Subjects are required to be literate and understand English. - Physically healthy. - Active duty military service, veterans, and their family members. Exclusion Criteria: - None

Study Design


Intervention

Behavioral:
CBT (Cognitive Behavior Therapy)
CBT group therapy sessions
EFT (Emotional Freedom Techniques)
Group therapy sessions using EFT

Locations

Country Name City State
United States Soul Medicine Institute Santa Rosa California

Sponsors (1)

Lead Sponsor Collaborator
Soul Medicine Institute

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change from Baseline PTSD (posttraumatic stress disorder) Symptom Levels Symptoms are measured before the first group therapy session. Symptom levels are also recorded immediately after the last group session, and at follow-up points: one, three, six, and twelve months later. Pre-Intervention, Post-Intervention, with one, three, six, and twelve month follow-ups
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