Psychological Symptom Change in Veterans After Six Sessions of EFT (Emotional Freedom Techniques)

Sponsor
Soul Medicine Institute (Other)
Overall Status
Completed
CT.gov ID
NCT01117545
Collaborator
(none)
59
1
2
91
0.6

Study Details

Study Description

Brief Summary

EFT (Emotional Freedom Techniques) has been shown to significantly reduce post-traumatic stress disorder (PTSD) and other psychological symptoms such as anxiety and depression in a variety of clinical trials. This study examines the effect of a six session EFT protocol on the symptoms of veterans with clinical scores on the PTSD Checklist-Military (PCL-M). Subjects in the experimental group receive EFT coaching supplemental to, and supportive of, the "usual care" treatment provided by their primary care provider. Subjects in the wait list control group receive usual care for a month, with pre and posttests, after which they also receive the EFT coaching protocol. Subjects are followed at three month intervals to determine if gains are maintained, and whether the symptom reductions are similar to those observed in other trials of EFT.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: EFT (Emotional Freedom Techniques)
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
59 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
Psychological Symptom Change in Veterans After Six Sessions of EFT (Emotional Freedom Techniques): A Randomized Controlled Trial
Actual Study Start Date :
May 1, 2010
Actual Primary Completion Date :
Jul 1, 2017
Actual Study Completion Date :
Dec 1, 2017

Arms and Interventions

Arm Intervention/Treatment
Experimental: EFT

Six sessions of EFT (Emotional Freedom Techniques)

Behavioral: EFT (Emotional Freedom Techniques)
Six sessions of EFT

No Intervention: Wait List

One month wait period

Outcome Measures

Primary Outcome Measures

  1. PTSD Scores on the PCL-M Assessment [One Month Before, At Start, After 3 and 6 Sessions, After 3 and 6 Months]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 90 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Military Service

  • The ability to follow instructions, complete written forms, and provide informed consent.

  • Remaining under the care of a primary care provider such as a VA hospital throughout the entire period of the study

  • Between 18 and 90 years old

Exclusion Criteria:
  • Participants with a score of more than 3 on questions 34 and 35 of the Symptom Assessment-45 Questionnaire (SA-45) will receive phone/skype sessions, not office visits

Contacts and Locations

Locations

Site City State Country Postal Code
1 Soul Medicine Institute Santa Rosa California United States 95404

Sponsors and Collaborators

  • Soul Medicine Institute

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

None provided.
Responsible Party:
Dawson Church, Executive Director, Soul Medicine Institute
ClinicalTrials.gov Identifier:
NCT01117545
Other Study ID Numbers:
  • SMI-PTSD-5410
First Posted:
May 5, 2010
Last Update Posted:
Apr 25, 2018
Last Verified:
Apr 1, 2018
Keywords provided by Dawson Church, Executive Director, Soul Medicine Institute
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 25, 2018