HBOTCSA: HBOT Effect on Chronic Pain Syndrome With a History of Psychological Trauma

Sponsor
Assaf-Harofeh Medical Center (Other)
Overall Status
Completed
CT.gov ID
NCT03376269
Collaborator
(none)
30
1
2
35
0.9

Study Details

Study Description

Brief Summary

The aim of the study is to evaluate the effect of hyperbaric oxygen therapy (HBOT) on 2 types of patients' population suffering from chronic pain syndrome (Fibromyalgia): patients with history of psychological trauma and patients with history of traumatic brain injury.

Condition or Disease Intervention/Treatment Phase
  • Biological: HBOT
  • Behavioral: Psychotherapy
N/A

Detailed Description

This study is a prospective clinical trial. After signing a written informed consent, all patients will be invited to medical evaluation including pain sensitivity examination and a series of questionnaires. In addition, all patients will have chest X-ray, cognitive evaluation, brain MRI and brain Single-photon emission computed tomography (SPECT)

. A second brain MRI, brain SPECT, pain sensitivity evaluation and questionnaires will be done after 3 months of treatment (60 sessions of HBOT). The HBOT procedure will be performed at the Sagol center for hyperbaric medicine and research of Assaf Harofeh Medical Center, Israel.

The following HBOT protocol will be applied for all patients: 12 weeks, 5 times per week, daily administration of 100% O2 for 90 minutes at a pressure of 2 absolute atmospheres (ATA) including 5 minutes air breaks every 30 minutes.

Patients with history of psychological trauma are also being treated with creative art psychotherapy. These patients will be randomly assigned to one of the two groups: (1) single intervention with creative art psychotherapy (psychotherapy group); (2) combined concurrent intervention of HBOT and creative art psychotherapy. Groups 1 will serve as controls during the first 3 months and then will be crossed to get HBOT. Before the cross to the HBOT they will have 2nd full evaluation (questioners and brain imaging).

Study Design

Study Type:
Interventional
Actual Enrollment :
30 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
The Effect of Hyperbaric Oxygen on Patients Suffering From Chronic Pain Syndrome (Fibromyalgia) With a History of Psychological Trauma
Actual Study Start Date :
Dec 1, 2014
Actual Primary Completion Date :
Jun 1, 2017
Actual Study Completion Date :
Nov 1, 2017

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Combined HBOT/psychotherapy

combined concurrent intervention of HBOT and creative art psychotherapy.

Biological: HBOT
•HBOT of 2 ATA for 90 minutes O2 100%, for 60 treatments

Behavioral: Psychotherapy
creative art psychotherapy which includes self drawing and daily diary alongside professional psychotherapy sessions

Other: psychotherapy

single intervention with creative art psychotherapy

Behavioral: Psychotherapy
creative art psychotherapy which includes self drawing and daily diary alongside professional psychotherapy sessions

Outcome Measures

Primary Outcome Measures

  1. Pain sensitivity [Change After 3 months]

    Using (AlogMed) dolorimeter, pain sensitivity will be examined in 18 trigger points (scale0-18)

  2. Brain microstructure [Change after 3 months]

    MRI dynamic tensor imaging sequence will be performed (DTI). Fractional anisotropy (FA) values will be assessed at base line and at 3 months. The changes at 3 months from baseline will be compared

  3. Brain Metabolism [Change after 3 months]

    Brain metabolism will be assessed using SPECT at baseline, 3 monthsThe counts for each different Broadmann area values will be calculated. The changes at 3 months from baseline will be compared.

Secondary Outcome Measures

  1. Fibromyalgia Impact on quality of life [Change after 3 months]

    Evaluated by Fibromyalgia Impact Questionnaire (FIQ).(scale 0-100)

  2. Quality of Life [Change after 3 months]

    Quality of live will be evaluated by Quality of Life RAND hort form 36 questionnaire (SF36).(scale 0-100)

  3. Stress [Change after 3 months t]

    Stress will be evaluated using the Perceived stress scale (PSS) questionnaire.(scale 0-51)

  4. Psychological symptoms [Change after 3 months]

    Psychological symptoms will be evaluated using Brief Symptom Inventory(BSI) questionnaire.(scale 0-20)

  5. Sensory symptoms [Change after 3 months]

    Sensory symptoms will be evaluated using the Sensory Profile questionnaires .

  6. Somatoform Dissociation Questionnaire (SDQ-20) [Change after 3 months]

    Dissociation symptoms will be evaluated using the Somatoform Dissociation Questionnaire (SDQ-20).

  7. Childhood trauma psychological effects [Change after 3 months]

    Childhood trauma psychological effects will be evaluated using the Childhood Trauma Questionnaire (CTQ) questionnaires.(scale 0-125)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Females

  • Age over 18

  • Known fibromyalgia (chronic pain syndrome) for more than 1 year

Exclusion Criteria:
  • Any past hyperbaric treatment prior to inclusion

  • Patients with chest x-ray pathology incompatible with hyperbaric environment

  • Patients with middle ear problems

  • Patients, who cannot "pump", equals middle ear pressure, effectively

  • Patients who suffer from claustrophobia

  • Inability or Refusing to sign the Informed Consent Form

Contacts and Locations

Locations

Site City State Country Postal Code
1 Assaf-Harofeh Medical Center Zerifin Israel 70300

Sponsors and Collaborators

  • Assaf-Harofeh Medical Center

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Prof. Shay Efrati, Director of Sagol Center for Hyperbaric medicine and Research, Assaf-Harofeh Medical Center
ClinicalTrials.gov Identifier:
NCT03376269
Other Study ID Numbers:
  • 202/14
First Posted:
Dec 18, 2017
Last Update Posted:
Dec 18, 2017
Last Verified:
Dec 1, 2017
Keywords provided by Prof. Shay Efrati, Director of Sagol Center for Hyperbaric medicine and Research, Assaf-Harofeh Medical Center
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 18, 2017