General Psychological Distress, PTSD, and Co-Morbidities in Healthcare Workers Consequent to Occupational Trauma

Recruiting now · Not applicable

Conditions studied: Post-traumatic Stress Disorder, Moral Injury

In brief

It is expected that large numbers of healthcare workers experience a broad range of psychological reactions and symptoms including anxiety, depression, moral distress, and trauma symptoms that will cause both significant suffering as well as occupational and social impairment. The purpose of this study is to find interventions which are helpful in treating psychological distress in healthcare workers adversely affected by occupational-related trauma. There are two phases of the study. All participants will take part in Phase I, which consists of 4 sessions over a two-week period of either a narrative writing intervention or a medical music intervention. Participants will be randomly assigned to the narrative writing intervention or medical music intervention. After Phase I, participants will be re-assessed. Healthcare workers who meet criteria for PTSD will be given the option to participate in Phase II of the study, in which they will be offered a choice between one of two evidence-based treatments for PTSD: Interpersonal Therapy (IPT) or Exposure Therapy (ET). Both treatments are comprised of ten 75-minute sessions scheduled twice weekly. Participants will be allowed to choose a preferred treatment in Phase II. After Phase II participants will complete a final assessment concluding the study. All interventions will be offered using distance technology.

Key facts

Study ID

NCT04626050

Run by

Weill Medical College of Cornell University

People needed

120

Starts

2022-01-20

Expected to finish

2028-04-01

Last updated by the study team

2026-06-22

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Any healthcare worker providing medical care or support who has experienced occupational-related trauma
• English-speaking
• Age >18
• Medically stable
• Able to provide informed consent and function at an intellectual level sufficient to allow accurate completion of all assessment instruments
• If on psychotropic medication stable for prior 60 days
• For phase II additional inclusion criteria:
• Current diagnosis of PTSD

You may not qualify if…

• Current significant unstable medical illness precluding regular session attendance or assessment completion
• Participants who in the investigator's judgment pose a current homicidal, suicidal, or other risk
• Lifetime or current diagnosis of schizophrenia or other psychotic disorder
• Participation in a clinical trial or concurrent evidence-based treatment for psychiatric conditions or PTSD during the previous 3 months.

Where it is running

• Weill Cornell Medicine — New York, New York, United States (enrolling)

Full record on ClinicalTrials.gov

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