A Recovery-Oriented Counselling Group

University of Calgary

Status: Completed

Conditions: Post-Intensive Care Recovery

Treatments: Behavioral: Counselling Group

Study type: Interventional

Funder types: Other

Identifiers

NCT03925181

REB18-2105

Details and patient eligibility

About

The purpose of this study is to evaluate a recovery-oriented group counselling program for post-discharged critical illness survivors and their caregivers.

Full description

The purpose of this pilot project is to develop and evaluate a recovery-oriented counselling group to support the physical, emotional, and social recovery processes of critical care survivors who access the services of the Calgary ICU Recovery Clinics. Upon discharge, critical care survivors are faced with challenges related to their stay in the Intensive Care Unit (ICU), as well as long-term recovery from critical illness. These challenges impact survivors' physical, emotional, social recovery processes, which reduce quality of life, delay (re)integration into their communities, and cause further health problems. Social support and counselling groups show therapeutic promise in supporting recovery processes by increasing social connection, quality of life, acquisition of skills, and emotional and psychological wellbeing.

The purpose of this study is to evaluate a recovery-oriented group counselling program for post-discharged critical illness survivors and their caregivers. The investigators will utilize Substance Abuse and Mental Health Service Administration's (SAMHSA) evidence-based recovery curriculum to develop a counsellor-facilitated recovery-oriented group for patients and caregivers focusing on peer support, relationships, evidence-based strategies, daily life, purpose and meaning-making, strengths, and resilience.

The research objectives are:

• Implement a recovery-oriented counselling group for ICU Recovery Clinic patients and their caregivers.
• Evaluate the recovery-oriented counselling group as situated within the Calgary ICU Recovery Clinic.

The investigators will utilize a Randomized Controlled Trial (RCT) design (non-clinical trial). Participants will be randomized into a treatment (intervention) or wait-list control group. Participants in the wait-list control group will be offered the intervention after the treatment group has completed the intervention group. The investigators will evaluate the intervention through the use of outcomes measures currently used by the ICU Recovery Clinic in a pre-test (t0), immediate post-test (t1), 3-month (t2), and 6-month (t3) follow-ups. In addition, the investigators will conduct a process evaluation of the intervention via content analysis of audio recorded data from semi-structured interviews and focus groups with participants. Patients and caregivers will participate in separate focus groups.

Enrollment: 17 patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria for Patients:

• Spent more than 4 days in the ICU,
• Were discharged into the community within 4 months of transfer out of the ICU (excluding patients who were in hospital long-term)
• Speaks English
• Has a fixed address
• Does not have pre-existing psychiatric diagnoses documented in the ICU transfer summary
• Lives within or surrounding Calgary.

Inclusion Criteria for Caregivers:

• Caregiver of an ICU survivor participant meeting criteria above
• Speaks English
• Has a fixed address
• Lives within or surrounding Calgary.

Exclusion Criteria for Patients:

• Long-term hospital stay

Excluding Criteria for Caregivers:

• None

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Single Group Assignment

Masking: None (Open label)

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17 participants in 2 patient groups

Intervention

Experimental group

Description:

Recovery counselling group.

Treatment:

Behavioral: Counselling Group

Waitlist control

No Intervention group

Description:

Waitlist control group. Will receive intervention after arm one is complete.