Pilot Study of a Multidisciplinary Intervention in ICU Survivors At Risk for Psychological or Physical Morbidity

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorRegion Stockholm

About this trial

Pilot study of the feasibility and utility of an early, in-hospital multidisciplinary intervention in ICU survivors at risk for psychological and physical problems post-ICU stay

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

None

Disqualifiers

Dementia or other major cognitive problems

Structural brain or spinal cord injury

Multiple limitations of medical treatment

Insufficient language skills (Swedish)

Trial design

Design model

Single group

Treatments tested in this trial

  • Case-manager led multidisciplinary follow-up after intensive care

    Other intervention

    Early in-hospital follow-up in survivors of intensive care with an increased risk of psychological/physical sequelae. The follow-up is led by a case-manager reassessing the patient after ICU discharge for psychological/physical rehabilitation needs. The CM will discuss patient needs with concerned specialists in a multidisciplinary team, leading to the establishment of a personal rehabilitation plan, communicated to the patient and next-of-kin. The CM will keep track of the patient during hospital stay and ensure primary care rehabilitation (if needed) is established once the patient is discharged from the hospital. The CM will contact the patient weekly to follow up on well-being and primary care activities until 12 weeks after discharge.

Treatment groups

60 Participants
are divided into 1 treatment group
Group A: Interventional armExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Feasibility of the intervention

Evaluation of the method including resource utilization with involved ICU follow-up staff/case managers and patients and their informal caregivers.

Time frame
Outcome measured during and after termination of data collection and end of intervention
2

Utility of the intervention

Patient and caregiver views on the intervention's utility. Views on the intervention from hospital ward staff.

Time frame
Outcome measured three-four months after ICU discharge

Secondary outcomes

1

Depressive symptoms post-ICU

Assessment of patients' symptoms of depression post-intervention

Time frame
Outcome measured three months after ICU discharge
2

Anxiety symptoms post-ICU

Assessment of patients' symptoms of anxiety post-intervention

Time frame
Outcome measured three months after ICU discharge
3

Symptoms of post-traumatic stress post-ICU

Assessment of patients' symptoms of post-traumatic stress post-intervention

Time frame
Outcome measured three months after ICU discharge
4

Physical disability post-ICU

Assessment of physical performance post-intervention

Time frame
Outcome measured three months after ICU discharge

Other outcomes

Sponsors and contacts

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