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Clinical Trials/NCT03503526
NCT03503526CompletedNot Applicable

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

Aalborg University0 sites45 target enrollmentStarted: August 13, 2015Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
45
Primary Endpoint
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).

Study Overview

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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
Female
Accepts 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.

Arms & Interventions

Music therapy treatment

Experimental

An intervention consisting of 12 weekly sessions of trauma-focused treatment in form of group music and imagery therapy.

Receptive music therapy.

Intervention: Receptive music therapy (Behavioral)

Wait List Control

No Intervention

No treatment for approximately 12 weeks.

Outcomes

Primary Outcomes

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).

Time Frame: 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 Outcomes

  • 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).)
  • 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).)
  • 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).)
  • 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).)
  • 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).)
  • 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).)
  • 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).)
  • 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).)
  • 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).)

Investigators

Sponsor
Aalborg University
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Gabriella Rudstam

Principal Investigator

Aalborg University

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