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Sleep Impairments in Refugees Diagnosed With PTSD

Sleep Impairments in Refugees Diagnosed With PTSD - A Polysomnographic and Self-report Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03535636
Acronym
PSG-PTSD
Enrollment
40
Registered
2018-05-24
Start date
2018-04-20
Completion date
2023-02-07
Last updated
2023-02-24

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

Conditions

PTSD, Sleep Disorder

Keywords

Polysomnography, Refugees

Brief summary

The aim of this study is to examine sleep architecture in refugees with PTSD. Polysomnography (PSG) will be carried out to study the occurrence of sleep disorders in patients and healthy controls.

Detailed description

There is little knowledge on treatment of sleep disturbances in trauma-affected refugees and this study will be the first to record the biophysiological changes that occur during sleep in refugees with PTSD. The study is a proof-of-concept study and this will contribute with new and potentially crucial knowledge of sleep disturbances in these patients. The project is designed as a cross-sectional study with 20 refugees with PTSD referred to the specialised outpatient clinic, Competence Centre for Transcultural Psychiatry (CTP), and 20 healthy control subjects. All patients referred to CTP will be invited to an initial consultation with a doctor. During this consultation a diagnostic assessment will be performed and the clinical history will be obtained. Patients who give informed consent will be invited to participate in the project and have sleep measurements performed by PSG. Furthermore self-administered questionnaires and semi-structured interviews will be used to collect information on mental health, sleep quality, sleep length and nightmares. Each patient will be equipped with PSG equipment to do measurements at home for one night (12 hours). Healthy control subjects will fill out the same CTP standard ratings and have the same diagnostic assessment and PSG measurement. The hypothesis is that the sleep architecture in refugees with PTSD differ from healthy controls. It is suggested that refugees with PTSD have increased dream activity as well as increased incidence of sleep disorders such as rapid eye movement (REM) sleep without atonia (RSWA), REM sleep behaviour disorder (RBD), sleep apnea and periodic limb movement disorder (PLM). The study is performed in collaboration with Danish Centre for Sleep Medicine in Denmark.

Interventions

OTHERPolysomnography

Sleep architecture will be assessed by polysomnography

Sponsors

Danish Center for Sleep Medicine
CollaboratorOTHER
Mental Health Services in the Capital Region, Denmark
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Adults (18 years old or above) * Refugee or family reunification refugees * PTSD according to the ICD-10 criteria's * Signed informed concent

Exclusion criteria

* Severe psychotic disorder (defined as patients with ICD-10 diagnoses F2x and F30.1-F30.9) * Harmful use of alcohol (ICD-10 diagnosis F1x.1) * Serious or progressive somatic illnesses that the lead investigator finds interfering for the study * Medical treatment with antipsychotics, benzodiazepine, opioids, CNS stimulants or regular use of anti histamine * BMI \>35 * Pregnancy

Design outcomes

Primary

MeasureTime frameDescription
Assessing the incidence of sleep disorders in refugees with PTSD12 hoursSleep architecture will be assessed by polysomnography. The recording of brain activity during sleep will reveal the incidence of sleep disorders such as sleep apnea, REM sleep without atonia and REM sleep behaviour disorder

Secondary

MeasureTime frameDescription
Harvard Trauma Questionnaire (HTQ)10 minutesAssessing PTSD symptoms
Hopkins Symptom Check List-25 (HSCL-25)10 minutesAssessing anxiety and depression symptoms
World Health Organization Well-Being Index (WHO-5)10 minutesAssessing subjective psychological well-being
Sheehan Disability Scale (SDS)10 minutesThe SDS is a brief, 5-item self-report tool that assesses functional impairment in work/school, social life, and family life. Total score 0-30 (0 unimpaired, 30 highly impaired). Work/school (0-10), Social life (0-10), Family life/home responsibilities (0-10). Scores of ≥5 on any of the 3 scales; high scores are associated with significant functional impairment.
Schedule for Clinical Assessment in Neuropsychiatry (SCAN)1 hoursDiagnosing and measuring mental illness that may occur in adult life.
Clinician Administered PTSD Scale (CAPS-5)1 hourAssessing PTSD symptoms, including their frequency and severity. The gold standard in PTSD assessment. The CAPS-5 is a 30-item structured interview and requires the identification of a single index trauma to serve as the basis of symptom inquiry. CAPS-5 total symptom severity score is calculated by summing severity scores for the 20 DSM-5 PTSD symptoms. Similarly, CAPS-5 symptom cluster severity scores are calculated by summing the individual item severity scores for symptoms corresponding to a given DSM-5 cluster: Criterion B (items 1-5); Criterion C (items 6-7); Criterion D (items 8-14); and, Criterion E (items 15-20). A symptom cluster score may also be calculated for dissociation by summing items 19 and 20. A patient needs to have: at least one Criterion B and C symptom and at least two Criterion D and E symptoms. Criterion F is met (disturbance has lasted one month) and Criterion G is met (disturbance causes either clinically significant distress or functional impairment).
Global Assessment of Functioning (GAF S + F)10 minutesA numeric scale used to subjectively rate the social, occupational, and psychological functioning of an individual
Hamilton anxiety scale (HAM-A14)15 minutesAssessing the severity of a patient's anxiety. The HAM-A probes 14 items. Each item is scored on a 5-point scale, ranging from 0=not present to 4=severe. Total score 0-56 (0 unimpaired, 56 highly impaired). The sum of all 14 items indicate the severity of anxiety; 14-17 = mild anxiety, 18-24 = moderate anxiety, 25-30 severe anxiety.
The Pittsburgh Sleep Quality Index (PSQI)10 minutesAssessing sleep quality and sleep disorders
Disturbing dreams and Nightmare Severity Index (DDNSI)10 minutesAssessing nightmares
REM Sleep Behavior Disorder Screening Questionnaire (RBDSC)10 minutesAssessing REM Sleep Behavior Disorders
Life Events Checklist for DSM-5 (LEC-5) - extended version10 minutesScreening of potential traumatic events
Hamilton depression scale (HAM-D17)15 minutesAssessing a patient's severity of depression before, during, and after treatment. The HAM-D probes 17 parameters. Some items are scored on a 5-point scale, ranging from 0=not present to 4=severe; others are scored on a 3-point scale, ranging from 0=not present to 2=severe. Total score 0-52 (0 unimpaired, 52 highly impaired). The sum of all 17 items indicate the severity of depression; 0-12 = normal, 13-17 = mild depression, 18-24 = moderate depression, 24-52 severe depression.

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 9, 2026