MedPath

Young People and Illness Management and Recovery (IMR)

Terminated
Conditions
Psychosis
Other Diagnoses and Conditions
Bipolar Disorder
Interventions
Behavioral: Illness management and recovery
Other: Semi-structured interviews
Registration Number
NCT04778085
Lead Sponsor
University Hospital, Akershus
Brief Summary

The study is a combined clinical patient outcome study and a health-services research sub-study. Illness management and recovery (IMR) constitutes an evidence-based practice with 11 modules focusing on personal recovery developed for adults with severe mental health illnesses. IMR can be offered in groups or individually, once a week for 10-12 months.

Little is known about how young people experience the utility of IMR treatment groups in child and adolescent mental health outpatient clinics. The primary aim is to explore in-depth how the participants experience the utility of the IMR approach. The health research sub-study will provide new insights into the IMR implementation process in outpatient clinics for adolescents.

Detailed Description

IMR has previously been implemented for adolescents in an inpatient unit in the hospital's catchment area. In order to offer the same treatment to all young patients, IMR treatment groups will be established in 4 out of 7 outpatient clinics in the hospital's catchment area. Participants belonging to the clinics in which no IMR treatment groups are being established will be invited to participate in IMR groups in clinics nearby.

The primary aim is to gain new insight into how young people experience the utility of IMR treatment groups conducted in outpatient practices and, if relevant, which changes could be made to adapt IMR more to young people. To explore how the participants experience the utility of IMR treatment groups, a qualitative focus-group study, consisting of a maximum of 5 focus-group interviews will be conducted. The participants in each IMR treatment group will be offered treatment once a week up to 10-12 months. To establish an IMR treatment group a minimum of 4 patients and a maximum of 8 participants must participate. Participants are mainly being included in the IMR treatment groups at the two primary admissions to each treatment group. Thus, some of the participants in the focus-groups may have participated in IMR groups for less than 10-12 months.

Secondary outcomes are related to fidelity to the model and the extent to which IMR treatment groups are implemented at an organizational level. The treatment groups will be led by trained IMR-therapists employed in inpatient units, together with therapists in training who are employed in outpatient clinics. Leaders and other clinicians in the outpatient clinics will contribute knowledge about the extent to which core components of IMR are being implemented, as well as information relating to quality improvement and individual adjustment. Two of the out-patient clinics in which no IMR group is being established will be included in the sub-study. The clinics will receive written feedback after each measurement time to support quality improvement.

The goal is to include up to 48 participants receiving IMR treatment in outpatient clinics. Up to 8 hospitalized participants will participate in a pilot focus-group interview. In the sub-study, a maximum of 16 IMR therapists, trained and in training, and up to 24 staff members will be invited to participate.

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
10
Inclusion Criteria

IMR therapists:

  • IMR therapist leading IMR treatment groups in one of the participating outpatient clinics
  • Trained or training in IMR
  • Employed at the Department for Child and Adolescent Mental Health Services at Akershus University Hospital.

Inclusion Criteria: Other staff members

• Employed at the Department for Child and Adolescent Mental Health Services at Akershus University Hospital.

Exclusion Criteria

Not provided

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
IMR patientsIllness management and recoveryPatients from outpatient clinics receiving IMR from trained IMR therapists and IMR therapists in training.
IMR therapists and other staffSemi-structured interviewsClinic leaders, IMR therapists and other staff participating in semi-structured individual or group interviews.
Primary Outcome Measures
NameTimeMethod
Focus-group interview aiming to explore the significance of the participant's own understanding of and knowledge about the disorder.End of treatment group, on average 11 months.

Focus-group interviews when the treatment group has come to an end aimed at exploring different perspectives on IMR treatment.

Focus-group interview aiming to explore the impact of the IMR treatment on dealing with everyday life.End of treatment group, on average 11 months.

Focus-group interviews when the treatment group has come to an end aimed at exploring different perspectives on IMR treatment.

Focus-group interview aiming to explore the importance of meeting other young people in the same situation.End of treatment group, on average 11 months.

Focus-group interviews when the treatment group has come to an end aimed at exploring different perspectives on IMR treatment.

Secondary Outcome Measures
NameTimeMethod
The Illness Management Fidelity ScaleBaseline (0 months), 6 and 12 months.

Assesses the degree of fidelity with 13 items on a 5-point Likert scale where 5 indicates full implementation and 0 indicates no implementation. Filled in by researchers on the basis of a semistructured interview with staff members.

The Illness Management and Recovery Scale (IMRS)Baseline (0 months), 6 and 12 months.

A 15-item scale that assesses illness self-management on a 5-point Likert scale where 5 indicates full self-management and 0 indicates no self-management. The scale measures consumer behavior relating to core components in the IMR program. The scale includes parallel clinician and consumer versions. Participants participating in IMR groups for less than 10-12 months will attend fewer measuring times.

Attendance registrationBaseline (0 months), 3, 6, 9 and 12 months.

The number of sessions the patients are attending in the IMR treatment group.

General Organizational IndexBaseline (0 months), 6 and 12 months.

A 12-item scale measuring organizational outcome of implementation, on a 5-point Likert scale where 5 indicates full implementation and 0 indicates no implementation. The scale is filled in by researchers on the basis of a semi-structured interview with staff members.

Trial Locations

Locations (1)

Akershus universitetssykehus

🇳🇴

Viken, Norway

© Copyright 2025. All Rights Reserved by MedPath