Prevalence of Post-traumatic Stress Disorder and Trauma Symptoms in a General Population Sample

Sponsor
Parc de Salut Mar (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05679245
Collaborator
(none)
50
5.9

Study Details

Study Description

Brief Summary

The goal of this observational study is to learn about how many people have post-traumatic stress disorder and related symptoms in the general population of people without any mental illness in the Barcelona region of Catalonia, Spain. The main questions it aims to answer are:

  • What is the prevalence of post-traumatic stress disorder in a sample of healthy controls without other mental disorders?

  • What is the prevalence of trauma-related symptoms in a sample of healthy controls without mental illness?

  • What is the prevalence of dissociative symptoms (including symptoms of depersonalisation and somatoform dissociation) in a sample of healthy controls without mental illness?

  • What is the prevalence of recent and childhood traumatic life events in a sample of healthy controls without mental illness?

  • What is the prevalence of difficulties in psychosocial functioning in healthy controls without mental illness?

  • What is the prevalence of depressive symptoms in healthy controls without mental illness?

  • What is the prevalence of general psychiatric symptoms in healthy controls without mental illness? Participants will be asked to take part in an online screening programme, and then to come to an interview with a clinician who will apply validated scales to test the above.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Assessment for exposure to psychological trauma and related symptoms

Detailed Description

This is a study to provide normative data for the prevalence of traumatic life events, post-traumatic stress disorder and trauma-related symptoms, and their impact on psychosocial functioning, and affective symptoms in healthy controls (i.e. without mental illness) in the Barcelona region of Catalonia, Spain.

Study Design

Study Type:
Observational
Anticipated Enrollment :
50 participants
Observational Model:
Ecologic or Community
Time Perspective:
Cross-Sectional
Official Title:
Prevalence of Post-traumatic Stress Disorder and Trauma-related Symptoms in a Sample of Healthy Controls in the Barcelona Region of Catalonia, Spain
Anticipated Study Start Date :
Feb 1, 2023
Anticipated Primary Completion Date :
Aug 1, 2023
Anticipated Study Completion Date :
Aug 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Healthy Controls

Healthy controls without mental disorder in the general population of the Barcelona area of Catalonia, Spain to be assessed for exposure to traumatic life events, post-traumatic stress disorder, trauma symptoms, dissociative symptoms, affective symptoms, and psychosocial functioning.

Diagnostic Test: Assessment for exposure to psychological trauma and related symptoms
To be assessed for exposure to traumatic life events, post-traumatic stress disorder, trauma-related symptoms, dissociative symptoms, affective symptoms, and psychosocial functioning.

Outcome Measures

Primary Outcome Measures

  1. Prevalence of post-traumatic stress disorder in a sample of healthy controls without mental disorder [cross-sectional, baseline]

    Prevalence of post-traumatic stress disorder according to criteria of the Diagnostic and Statistical Manual of Mental Disorders - 5th Edition, as per the Global Evaluation of Post-traumatic Stress Disorder Scale (EGEP-5), which assesses the presence or absence of post-traumatic stress disorder.

  2. Prevalence of trauma symptoms in a sample of healthy controls without mental disorder [cross-sectional, baseline]

    Prevalence of trauma-related symptoms according to the Impact of Events Scale-Revised (IES-R), which is scored on a Likert scale with a maximum score of 110, with higher scores meaning a greater level of trauma symptoms.

  3. Prevalence of dissociative symptoms in a sample of healthy controls without mental disorder [cross-sectional, baseline]

    Prevalence of dissociative symptoms according to the Dissociative Experiences Scale (DES). The final score is out of 100, with higher scores meaning a greater number of symptoms.

Secondary Outcome Measures

  1. Prevalence of depressive symptoms in a sample of healthy controls without mental disorder [cross-sectional, baseline]

    Prevalence of depressive symptoms according to the Hamilton Depression Rating Scale (HDRS), which can provide a total score between 0 and 63, with higher scores meaning greater depressive symptoms.

  2. Prevalence of psychiatric symptoms in a sample of healthy controls without mental disorder [cross-sectional, baseline]

    Prevalence of psychiatric symptoms according to the Brief Psychiatric Rating Scale (BPRS). The first 18 items on this scale provide a total score from 0 to 146, with higher scores signifying more severe psychiatric symptoms, while item 19 provides an estimate of severity of illness on a Likert scale from 1 to 7.

  3. Prevalence of symptoms of somatoform dissociation in a sample of healthy controls without mental disorder [cross-sectional, baseline]

    Prevalence of symptoms of somatoform dissociation according to the Somatoform Dissociation Questionnaire (SDQ-20). Each item is scored on a Likert scale from 1 to 5, up to a total score of 100. Higher scores denote more somatoform symptoms.

  4. Prevalence of depersonalisation dissociative symptoms in a sample of healthy controls without mental disorder [cross-sectional, baseline]

    Prevalence of depersonalisation dissociative symptoms according to the Cambridge Depersonalisation Scale. Each item is scored for frequency (0 to 4) and duration (1 to 6), and these scores are summed together to create a total score. Higher scores indicate greater levels of dissociative symptoms.

  5. Prevalence of difficulties in psychosocial functioning in a sample of healthy controls without mental disorder [cross-sectional, baseline]

    Prevalence of difficulties in psychosocial functioning according to the Functioning Assessment Short Test (FAST). Each item on this scale is scored on a Likert scale of 0 to 3, providing a total score between 0 and 72. Higher scores indicate a greater degree of difficulty in functioning.

  6. Prevalence of childhood trauma events (physical, sexual, or emotional abuse, and physical or emotional neglect) in a sample of healthy controls without mental disorder [cross-sectional, baseline]

    Prevalence of childhood trauma experiences according to the Childhood Trauma Questionnaire (CTQ). This scale provides a score for each subscale of physical, sexual, or emotional abuse, and physical or emotional neglect, with scores categorised as ranging from none to severe.

  7. Prevalence of recent stressful life events in a sample of healthy controls without mental disorder [cross-sectional, baseline]

    Prevalence of recent stressful life events in the previous year according to the Social Readjustment Rating Scale (Holmes & Rahe). This scale provides the number of stressful events. Each event has a weighted score which is summed to create a total score, with higher scores signifying a greater risk of stress-related illness.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • to be an adult (18-65 years inclusive)
Exclusion Criteria:
  • to have a mental disorder except for post-traumatic stress disorder, determined by application of the Mini International Neuropsychiatric Interview (MINI)

  • active suicidal ideation

  • presence of organic brain disease

  • presence of somatic diseases such as fibromyalgia or chronic fatigue syndrome

  • presence of autoimmune diseases such as HIV or AIDS

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Parc de Salut Mar

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Parc de Salut Mar
ClinicalTrials.gov Identifier:
NCT05679245
Other Study ID Numbers:
  • CS01
First Posted:
Jan 10, 2023
Last Update Posted:
Jan 10, 2023
Last Verified:
Dec 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Parc de Salut Mar
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 10, 2023