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Clinical Trials in Germany / NCT06733493
Active, not recruiting Not applicable

Study Protocol for a Pilot Randomized Controlled Trial of a Psychosocial Care Intervention in Intensive Care

NCT06733493 · tracked via the Priya Life Science Germany tracker
Sponsor
Harald Gündel
Phase
Not applicable
Started
2024-08-01
Last updated
2025-07-01

Condition(s) studied

Psychosocial InterventionIntensive Care Units (ICUs)Psychosocial Health

Investigational drug(s) / intervention(s)

integrated psychosocial care

integrated psychosocial care: Employment of a psychologist in psychotherapeutic training as a member of the multiprofessional team at the ICU ward for the duration of one year. Tasks: Psychosocial Support for staff, patients and their relatives.

Study summary

This Pilot-RCT is part of a feasibility study that aims to learn if the IPS-psychosocial care intervention and an RCT on its efficacy are feasible in patients, relatives and staff on icu wards. The Pilot-RCT will examine outcomes, that might indicate an improvement in psychosocial safety climate and other health- and wellbeing-related measures due to the administration of the intervention that is described in the following. The main question the Pilot-RCT aims to answer is:

Is there evidence that the IPS intervention improves the psychosocial safety climate and other components of psychosocial well-being in ICU teams, patients and their relatives?

Researchers will compare four intervention groups (icu wards with implementation of the IPS-Intervention) with four control groups (icu wards with regular supply of psychosocial care) to see if the comparison of two groups in this RCT is feasible.

The IPS-Intervention consists of a ward psychologist who works as part of the ICU team and takes care of the staff, patients and relatives in accordance to the intervention manual that was developed in a prior phase of this project.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * Affiliation to one of the 8 participating ICU wards during the duration of the study, either by: occupation as a healthcare professional, admission as a patient, relation to an admitted patient Exclusion Criteria: * Age under 18 years old * Inability to give informed consent

Primary outcome measure(s)

Trial sites (4)

FacilityCityRegionStatus
Clinic of Psychosomatic Medicine and Psychotherapy, University Hospital Ulm Ulm Baden-Wurttemberg
Psychosomatic Medicine and Psychosomatic Therapy, Medical Faculty University Hospital Magdeburg Magdeburg Saxony-Anhalt
Institute of Social Medicine and Health Systems Research (ISMHSR) Magdeburg Saxony-Anhalt
Medical Clinic - Department of Psychosomatic Medicine of the Charité Berlin State of Berlin
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06733493 on ClinicalTrials.gov ↗ ← All trials in Germany