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N/A N=555 Randomized Single-blind Health Services Research

Randomized Controlled Trial of Wellness Recovery Action Planning

Mental Disorders

Enrolled (actual)
555
Serious AEs
0.0%
Results posted
Jan 2020
Primary outcome: Primary: Psychiatric Symptoms Recovery Using the Brief Symptoms Inventory (BSI) — 20.6; 19.29; 19.52; 21.38 symptom severity score — p=0.027

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Wellness Recovery Action Planning (WRAP) (Behavioral)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
University of Illinois at Chicago
Primary completion
Sep 2009

Outcome Measures

OutcomeResultp-value
PRIMARY
Psychiatric Symptoms Recovery Using the Brief Symptoms Inventory (BSI)
20.6; 19.29; 19.52; 21.38; 12.20; 12.65 0.027 sig
PRIMARY
Hopefulness
21.67; 21.87; 22.47; 22.07; 22.76; 22.16 0.020 sig
PRIMARY
Patient Self-Advocacy
3.47; 3.46; 3.61; 3.53; 3.65; 3.55 0.029 sig
PRIMARY
Recovery From Mental Illness
88.2; 87.4; 92.9; 90.0; 93.7; 91.2 0.042 sig
SECONDARY
Quality of Life Brief Assessment
13.1; 13.1; 13.7; 13.5; 14.1; 13.4 .001 sig

Summary

The purpose of this research study is to test the effectiveness of a standardized peer-led intervention to teach self-management skills in improving outcomes of individuals with a severe mental illness. The intervention is known as Wellness Recovery Action Planning or WRAP, co-developed by Dr. Mary Ellen Copeland. The focus of the inquiry is on whether and how developing an individualized plan for successful living: 1) lowers psychiatric symptoms; 2) enhances psychosocial outcomes such as self-perceived recovery, empowerment, self-advocacy, coping, and social support; 3) increases knowledge of personal mental illness self-management strategies; and 4) enhances satisfaction with the service delivery system. The study evaluated the following hypotheses: Hypothesis #1: Compared to wait-list control subjects, those who participate in the WRAP intervention will report reduced levels of psychiatric symptoms. Hypothesis #2: Compared to wait-list control subjects, those who participate in the WRAP intervention will report enhanced enhanced feelings of empowerment, hope, recovery, quality of life, and functioning. Hypothesis #3: Compared to wait-list controls, those who participate in the WRAP intervention will report increased levels of social support. Hypothesis #4: Compared to wait-list controls, those who participate in the WRAP intervention will report increased use of peer services, higher satisfaction with services, and have lower overall service costs. Hypothesis #5: Compared to controls, those who participate in the WRAP intervention will report increased knowledge of mental illness self-management, including making/using a WRAP plan. Hypothesis #6: There will be no difference in employment rates of control vs. intervention subjects.

Eligibility Criteria

Inclusion Criteria

  • age 18 years or older
  • English speaking
  • severe mental illness as confirmed by: 1) a Kessler Self-Report Measure (K-6) score of 13 or higher; and/or 2) enrolled as a client of the public mental health system in the state of Ohio.

Exclusion Criteria

  • non English speaking
  • not meeting clinical criteria for severe mental illness
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01024569). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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