Peer Support for Post Intensive Care Syndrome Self-Management

Status unconfirmed · Not applicable

Conditions studied: Critical Illness, Sepsis, Shock, Septic, Shock, Respiratory Failure, Respiratory Distress Syndrome, Adult, Shock, Hypovolemic, Chronic Disease

In brief

A prospective, 2-arm, single-blind, randomized controlled clinical feasibility trial design is planned. Forty CCI survivors will be randomized (1:1) to either the PS-PICS (peer support) intervention or usual care (control) group.

Key facts

Study ID

NCT03788096

Run by

University of Texas at Austin

People needed

40

Starts

2020-04-20

Expected to finish

2021-01-27

Last updated by the study team

2020-11-02

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• age18 years or older
• ICU length of stay 8 days or longer
• expected to survive hospitalization with a discharge destination to home within 28 days of hospital discharge
• diagnosed with 2 or more chronic conditions.

You may not qualify if…

• death prior to hospital discharge
• enrollment in Hospice services at the time of hospital discharge
• non-communicative
• no access to telephone
• incarcerated

Where it is running

• Baylor Scott & White Health — Temple, Texas, United States (enrolling)

Full record on ClinicalTrials.gov

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