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N/A N=250

Assessing Mental Illness Recovery

Serious Mental Illness

Enrolled (actual)
250
Serious AEs
3.6%
Results posted
Jan 2017
Primary outcome: Primary: Positive and Negative Symptom Scale (PANSS) — 1.9; 1.8 units on a scale

Study Design & Population

Study type
Observational
Phase
N/A
Interventions
Age
Adult, Older Adult · 25+ yrs
Sex
All
Sponsor
VA Office of Research and Development
Primary completion
Jul 2013

Outcome Measures

OutcomeResultp-value
PRIMARY
Positive and Negative Symptom Scale (PANSS)
1.9; 1.8
SECONDARY
Maryland Assessment of Recovery in Serious Mental Illness
95.9; 95.7

Summary

In 2003 the VA Undersecretary's Action Agenda mandated that mental health services throughout the system be transformed to a recovery model. That mandate and many of the Workgroup recommendations have since been formalized in the Uniform Mental Health Services Package, which specifies a range of recovery-oriented services that must be available to veterans. A key aspect of these policy mandates is the need to assess recovery status of veterans and to monitor their progress over time as a way to evaluate the effectiveness of recovery services. However, there is no established instrument that is suitable for system-wide application. The purpose of this project is to develop a reliable, valid and practical measure of recovery, and use the measure in a study to better understand recovery in individuals with serious mental illness.

Eligibility Criteria

Inclusion Criteria

  • chart diagnosis of schizophrenia, schizoaffective disorder, bipolar disorder I (with mania), or major depression with psychotic features, with a history of a minimum of 2 psychotic exacerbations, or Psychosis NOS
  • A minimum of 2 psychotic exacerbations(confirmed by medical record, provider report, or patient self-report);
  • Are receiving services from participating study sites and have had a minimum of two service visits within the last 6 months;
  • Have received mental health services for a minimum of 3-years;
  • Age between 25 and 65;
  • Able to provide informed consent; and
  • Able to complete protocol assessments (estimation from medical record and/or mental health provider that person can read at 5th grade level and sustain attention to study tasks for required period of time).

Exclusion Criteria

  • Severe or profound mental retardation as indicated by chart review
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01043653). 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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