ICU-SUCCEED for Survivors of Acute Respiratory Failure and Their Caregivers

Part of paid clinical trials in Chapel Hill, North Carolina.

Sponsor
University of North Carolina, Chapel Hill
Study ID
NCT07778004
Status
Not Yet Recruiting

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Conditions

  • Acute Respiratory Failure
  • Critical Illness
  • Hypercapnia
  • Hypoxia
  • Sepsis

Eligibility Criteria

Sex
ALL
Age
18 Years - 99 Years
Healthy Volunteers
Not accepted

Interventions

  • ICU-SUCCEED — BEHAVIORAL
    Includes one inpatient (in-person) session followed by four outpatient (Zoom or telephone) sessions. Dyads will receive one session every 1-2 weeks. Each session will have a different focus, which may incorporate one of the following: communication, self-management, emotion management, stress management, lifestyle and hobbies, and interpersonal relationship building. This intervention has been adapted to meet the needs of patients with acute respiratory failure and their caregivers
  • Augmented Usual Care — OTHER
    Usual care will continue unchanged and will include any services, counseling, monitoring, or referrals that are coordinated by the clinical team prior to discharge. Handouts include a hospital discharge preparation checklist and information about the long-term complications of and recovery from critical illness.

Study Details

This study will investigate whether a family-centered intervention that has been adapted for patients with critical illness and their caregivers is possible, acceptable, and helpful

Key Dates

First listed
Aug 21, 2026
Start date
Sep 1, 2026
Status verified
Aug 2026
Primary completion
Sep 1, 2030
Completion
Sep 1, 2030

Study Design

Enrollment
144 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE

Arms

  • Experimental: ICU-SUCCEED
    This arm will receive ICU-SUCCEED intervention.
  • Placebo Comparator: Augmented Usual Care
    This arm will receive standard care routinely available plus written handouts prior to hospital discharge.

Primary Outcome Measure

Feasibility of participant eligibility [ Time Frame: From the start to the end of recruitment ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
UNC HospitalsChapel HillNorth Carolina27599
Blair Wendlandt, MD, MSCR
[email protected]
984-542-7702

Find similar trials in Chapel Hill, NC

By research site
UNC Hospitals· Chapel Hill, NC

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