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Trauma-focused Group Music and Imagery With Traumatized Women

Trauma-focused Group Music and Imagery With Women Suffering From PTSD/Complex PTSD

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03503526
Enrollment
45
Registered
2018-04-20
Start date
2015-08-13
Completion date
2018-08-22
Last updated
2021-01-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stress Disorders, Post-Traumatic

Brief summary

This study is a mixed methods randomized controlled trial (Wait List Control), that investigates the effects of Group Music and Imagery (GrpMI) therapy in the treatment of women suffering from Post Traumatic Stress Disorder (PTSD) or Complex PTSD. The aim is to detect if the intervention has an effect on PTSD symptoms, dissociation, quality of life, and the capability of regulating the autonomic nervous system (ANS).

Detailed description

Participants are adult women suffering from PTSD or Complex PTSD (n=56) that are randomized to three months of weekly (12) sessions of trauma modified GrpMI therapy or no treatment for an equal amount of time (wait list control). Primary outcome is pre, post and 3 months follow-up measures of PTSD checklist 5 (PCL-5). Secondary outcome is pre, post and 3 months follow-up measures of dissociative experience scale (DES), positive state of mind scale (PSOM-S), Hopkins symptoms checklist (HSCL-25), somatoform dissociation questionnaire (SDQ-5), and reactivity and recovery of different physiological measures related to arousal regulation ability in a script driven imagery setting.

Interventions

12 weekly trauma-focused Group therapy sessions of a length of 2.5 hours. The core element is receptive music psychotherapy with music listening, art making, and other art based methods.

Sponsors

Kris- och Traumacentrum Sverige AB
CollaboratorUNKNOWN
Council of the Danish Victims Fund
CollaboratorUNKNOWN
Aalborg University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

A randomized wait list control study with a mixed methods design

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* be suffering from PTSD/CPTSD, * be sufficiently stabilised to tolerate being exposed to trauma treatment and listen to other subjects' stories, * be able to speak good enough swedish to express themselves without an interpreter, * have an interest in working with their problems using artistic languages, * have an ability to work with symbolism and inner images.

Exclusion criteria

* difficulties in understanding or making themselves understood in swedish, * severe personality disorder or neuropsychiatric disorder, * ongoing alcohol or drug abuse, * psychotic disorder, * suicidality, * serious ongoing medical condition, * serious psychosocial problems.

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline in Posttraumatic Stress Disorder Checklist (version 5) (PCL-5) total score at 3 months (post intervention) and at 6 months (follow- up).Baseline, 3 months (post intervention) and 6 months (follow- up).PCL-5 is a 20-item self-assessment scale, measuring symptoms related to posttraumatic stress disorder (PTSD). The total score range are from 0-80. Higher scores indicate more severe PTSD symptoms.

Secondary

MeasureTime frameDescription
Change from baseline in Hopkins symptom checklist (HSCL-25) mean scores at 3 months (post intervention) and at 6 months (follow- up).Baseline, 3 months (post intervention) and 6 months (follow- up).HSCL-25 is a 25-item self-assessment scale with two subscales. The first subscale measures anxiety and has 10 items. Each item ranges from 1 to 4. The mean score is used as an index of anxiety. A high mean score indicates more anxiety symptoms. The second subscale measures depression and has 15 items. Each item range from 1 to 4. The mean score is used as an index of depression. Higher mean score indicate more depressive symptoms.
Change from baseline in Positive states of mind scale (PSOM-S) total score at 3 months (post intervention) and at 6 months (follow- up).Baseline, 3 months (post intervention) and 6 months (follow- up).PSOM-S is a 5-item self-assessment scale that measures quality of life. The total range are from 5-15. Higher scores indicate a higher quality of life.
Change from baseline in Somatoform Dissociation Questionnaire (SDQ5) total score at 3 months (post intervention) and at 6 months (follow- up).Baseline, 3 months (post intervention) and 6 months (follow- up).SDQ5 is a 5-item self-assessment scale that measures somatoform dissociation. The total range are from 5-15. Higher scores indicates more severe somatoform dissociative symptoms.
Change from baseline in timeline of heart rate during exposure to script-driven trauma imagery at 3 months (post intervention) and 6 months (follow-up).Baseline, 3 months (post intervention) and 6 months (follow- up).Heart rate (bpm) measured with a blood volume pulse sensor.
Change from baseline in Dissociative experience scale (DES) mean score at 3 months (post intervention) and at 6 months (follow- up).Baseline, 3 months (post intervention) and 6 months (follow- up).DES is a 28-item self-assessment scale that measures psychoform dissociation. Each item ranges from 0 % to 100 % and the mean score is used as an index for the severity of the dissociative symptoms. A higher mean score indicates more dissociative symptoms.
Change from baseline in timeline of skin conductance level during exposure to script-driven trauma imagery at 3 months (post intervention) and 6 months (follow-up).Baseline, 3 months (post intervention) and 6 months (follow- up).Measured with electrodes on the proximal phalanges of the left hand´s index and ring finger.
Change from baseline in timeline of muscle tension during exposure to script-driven trauma imagery at 3 months (post intervention) and 6 months (follow-up).Baseline, 3 months (post intervention) and 6 months (follow- up).Measured as root mean square amplitude of the electromyography signal (micro volt) with electrodes placed on the left forearm (over the extensor digitorum muscle).
Change from baseline in timeline of the root mean square of successive differences (RMSSD) in intervals between individual heart beats during exposure to script-driven trauma imagery at 3 months (post intervention) and 6 months (follow-up).Baseline, 3 months (post intervention) and 6 months (follow- up).Derived from the heart rate time series using the beat-to-beat peak blood volume-intervals (measured with a plethysmograph on the right middle finger).
Change from baseline in timeline of peripheral temperature during exposure to script-driven trauma imagery at 3 months (post intervention) and 6 months (follow-up).Baseline, 3 months (post intervention) and 6 months (follow- up).Temperature measured on the fingertip of the left hand´s middle finger.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026