Post-traumatic Stress Disorder Clinical Trial
Official title:
Effectiveness of Thought Field Therapy Provided by Community Workers to a Traumatised Population in Uganda: a Randomised Trial
Thought Field Therapy (TFT) is a simple technique that involves tapping on points of the
body corresponding to the meridians used in acupuncture. By using specific sequences, TFT
can be used to treat a variety of psychological problems. Patients can be taught to treat
themselves, and lay people can be trained to treat others in their community, as has been
shown for narrative exposure therapy.
Thought Field Therapy has been used to treat whole communities who have suffered
psychological trauma following natural disasters and violent conflicts. In these
circumstances, TFT can be used as a stand-alone therapy, or as an adjunct to other
psychological therapies, by removing the pain of re-living the traumatic events.
Studies in Rwanda have shown that individuals within a community can be treated with brief
TFT sessions. Both short-term and longer-term improvements in scores of Post-Traumatic
Stress Disorder (PTSD) measurement scales have been demonstrated.
The Kasese District has suffered from factional conflicts and the consequences of the
ongoing struggles in neighbouring countries for many years. Although the government has
controlled the situation and secured the borders, many are still haunted by the
psychological consequences.
The purpose of the study is to validate the model of addressing widespread psychological
trauma following conflict by training community leaders to help others in their community
using TFT.
Thirty-six community leaders will be given a two-day training in algorithm level
trauma-relief TFT. They will then treat 128 volunteers for their traumas, using TFT, who
will be assessed before and after treatment by the post-traumatic stress disorder check-list
questionnaire for civilians (PCL-C). As a control, a further 128 volunteers will join a
wait-list group, who will be assessed at the same time, but treated later.
PCL-C scores before and after treatment will be compared with the wait-list group scores
before and after waiting, but before their treatment.
A follow-up assessment of the participants will be undertaken 1 to 2 years later.
Six TFT practitioners from the USA, Great Britain, and Norway will train 36 community
leaders during a two-day trauma-relief training programme. These newly-trained practitioners
will then treat 256 volunteers who feel that they are suffering from psychological trauma.
The six visiting practitioners, together with two additional TFT practitioners from Rwanda,
will supervise and support the study following the training.
A Catholic Priest, Father Peter Mubunga Basaliza, on behalf of the Kasese Diocese, will
organise the recruitment of the local trainers and volunteer participants, including
publicising by local radio. All faiths will be welcome, but volunteers must be 18 years of
age or older. Volunteers will be informed of their allocated date and time to attend for
inclusion in the study. Any volunteer who cannot be accommodated in the study because the
pre-requisite number has been met, will be offered TFT by the visiting practitioners and
trained community leaders.
Signed consent will be obtained prior to commencing the study. Participants will be provided
with an information sheet and duplicate consent forms in Lhukonzo (the local language), and
assistance will be provided by Ugandan therapists for those who have difficulty reading it.
Consent forms will also be available in English for those for whom it is the preferred
language. Each participant will also complete a demographic questionnaire.
Participants will be free to withdraw at any time, and any who do will still be offered TFT,
if desired.
Sixty-four participants will be seen each day, 32 in the morning, and 32 in the afternoon,
for four consecutive days. They will be alternately allocated to Group A and provided with a
blue folder, or Group B and provided with a red folder. Their names will be recorded on a
sign-in sheet. They will be identified by a number, which will be written on their folder
and documents. Both groups will initially complete the post-trauma checklist (PCL-C)
questionnaire (www.pdhealth.mil) available in Lhukonzo, referring to symptoms within the
previous week. Therapists, who will be unaware of the individual's group allocation, will
assist if necessary. The PCL-C has been translated from English into Lhukonzo and back into
English to ensure that the translation is accurate.
Completed questionnaires and consent forms will be kept in their folders and retained by the
researchers.
Following completion of the PCLs, Group A participants will be treated using Thought Field
Therapy by the newly trained therapists for their traumas, supervised by the researchers.
The therapists will keep a record for each participant of the problem that was treated,
algorithms used, the time taken, and the Subjective Units of Distress (SUD) scores (0-10).
Group B will be a control (wait-list group) and will receive no treatment following their
first visit. This model has been successfully utilised in Rwanda.
One week later, at the same time and day of the week as they first attended, the
participants in group A and group B will return and repeat their PCL. On this occasion,
testing will be followed by treatment for Group B.
After a further week, Group B only will return for repeat testing using PCL.
In summary, the protocol to be followed will be:
- Two-day training of new therapists
- Day one of study: 9am - PCL test of 16 Group A and 16 Group B 11am -Treat the 16 Group
A
1pm - Test a new group of 16 A and 16 B 3pm - Treat the new 16 group A
- Days 2-4: Same as for day one, but with new participants. Each therapist will treat the
same number in each group.
- Days 8-11 9am -PCL test of 16 Group A and 16 Group B 11am -Treat the 16 Group B
1pm - Test another 16 of each Group 3pm -Treat the new Group B
- Day 18 Test all Group B, 16 every two hours from 9am
Mean + SD PLC test scores will be calculated for each group during their four days of each
week, and of Group B on day 18. That is:
Group A days 1-4 (A pre-treatment) Group B days 1-4 (B pre-treatment) Group A days 8-11 (A
post-treatment) Group B days 8-11 (B post-no treatment) Group B day 18 (B post-treatment)
The statistical significance of differences of mean scores will be analysed by analysis of
variance and paired samples t tests.
Statistically significant differences were found in a similar study in Rwanda, with smaller
numbers, so the study will be adequately powered.
A follow-up assessment will be done 19 months later.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Caregiver), Primary Purpose: Treatment
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT04317820 -
Deep Brain Reorienting in Post-traumatic Stress Disorder
|
N/A | |
Completed |
NCT05112003 -
Translingual Neurostimulation for the Virtual Treatment of Post-Traumatic Stress Disorder: A Feasibility Pilot
|
N/A | |
Recruiting |
NCT04518267 -
Anger and Psychotrauma: Data From Military and Civilians
|
||
Completed |
NCT02502604 -
Cognitive Training Program for Individuals With Depression and Post-Traumatic Stress Disorder
|
N/A | |
Completed |
NCT02256566 -
Cognitive Training for Mood and Anxiety Disorders
|
N/A | |
Terminated |
NCT02234687 -
A mGlu2/3 Agonist in the Treatment of PTSD
|
Phase 1 | |
Completed |
NCT02213900 -
Preventing Post-Operative Delirium in Patients Undergoing a Pneumonectomy, Esophagectomy or Thoracotomy
|
Phase 4 | |
Terminated |
NCT02520726 -
PTSD Prevention Study Examining the Efficacy of Sertraline in Burn Victims
|
Phase 4 | |
Completed |
NCT01738308 -
The Effects of Healing Touch on Post Operative Pediatric Patients
|
N/A | |
Completed |
NCT01437891 -
Sentra AM® and Sentra PM® for Post-traumatic Stress Disorder (PTSD) and Gulf War Fibromyalgia (GWF)
|
N/A | |
Completed |
NCT01517711 -
Tramadol Extended-Release (ER) for Posttraumatic Stress Disorder (PTSD)
|
Phase 4 | |
Completed |
NCT01998100 -
Maximizing Treatment Outcome in Post-Traumatic Stress Disorder (PTSD)
|
Phase 3 | |
Completed |
NCT01199107 -
Maximizing Treatment Outcome and Examining Sleep in Post-traumatic Stress Disorder (PTSD)
|
Phase 3 | |
Completed |
NCT01231711 -
Improving Quality-of-life and Depressive Symptoms of Combat Veterans Via Internet-based Intervention
|
Phase 1 | |
Completed |
NCT00680524 -
Telephone-based Care for OEF/OIF Veterans With PTSD
|
N/A | |
Completed |
NCT00348036 -
Group Intervention for Interpersonal Trauma
|
N/A | |
Completed |
NCT00838006 -
Psychophysiologic Predictors of Post-deployment Mental Health Outcomes
|
N/A | |
Completed |
NCT00525226 -
Evaluating the Effects of Stress in Pregnancy
|
N/A | |
Completed |
NCT00158262 -
Effect of Propranolol on Preventing Posttraumatic Stress Disorder
|
Phase 4 | |
Completed |
NCT00127673 -
Comparison of Two Treatments for Post-Traumatic Stress Disorder
|
Phase 3 |