posttraumatic stress disorder trauma
Conditions
Interventions
None listed
Sponsors
Universitair Medisch Centrum Utrecht
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: male, age 18-65, CAPS > 50 (patients)
Exclusion criteria
Exclusion criteria: substance /alcoholabuse within 6 months psychotrophic medication chronical benzodiazepin use History of psychiatric disorder (controls), CAPS > 18 (contorls)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome measure is number of awakenings of plasma cortisol concentrations. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary objectives are 1. Other PSG parameters 2. Nocturnal excretion of catecholamines and hormones of the HPA axis in 3. Correlations of plasma concentration of catecholamines and hormones of the HPA axis with number of arousals and other PSG parameters 4. Correlation of subjective sleep complaints with number of awakenings and other PSG parameters 5. Correlation of objective and subjective sleep quality with general psychological and somatic well being, according to *Symptom Checklist - 90* (SCL-90) and *Checklist Individuele Spankracht* (CIS). 6. Correlation of sleep endocrinology with temperament and personality, as measured by *Temperament and Character Inventory*. 7. Awakening response curve of cortisol and ACTH in PTSD compared with controls | — |
Countries
Netherlands
Outcome results
None listed