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N/A N=240 Supportive Care

The Effectiveness of a Decision-Support Tool for Adult Consumers With Mental Health Needs and Their Care Managers

Mental Disorders

Enrolled (actual)
240
Serious AEs
4.2%
Results posted
Apr 2017
Primary outcome: Primary: Short Form Health Survey-12 (SF-12), Physical Symptoms Subscale — 38.167; 38.601; 37.187; 37.108 units on a scale — p=.0679

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Moving Patient Outcomes toward Wellness and Recovery (mPOWR) (Behavioral)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Felton Institute
Primary completion
Oct 2016

Outcome Measures

OutcomeResultp-value
PRIMARY
Short Form Health Survey-12 (SF-12), Physical Symptoms Subscale
38.167; 38.601; 37.187; 37.108; 34.386; 35.884 .0679
PRIMARY
Short Form Health Survey-12 (SF-12) Mental Symptoms
43.828; 38.647; 34.153; 39.970; 39.931; 39.570 .0988
PRIMARY
Outcome Rating Scale (ORS)
58.085; 49.003; 57.522; 59.583; 54.083; 56.987 .6588
PRIMARY
Shared Decision Making Questionnaire
4.698; 4.005; 4.995; 5.220; 4.512; 4.363 .5840
PRIMARY
Working Alliance Inventory
5.896; 5.494; 6.203; 6.058; 5.842; 5.810 .9046
PRIMARY
Communication Satisfaction Questionnaire
4.283; 4.024; 4.363; 4.473; 3.947; 4.093 .0283 sig

Summary

The primary goal of the proposed study is to investigate the implementation and effectiveness of the mPOWR (Moving Patient-centered Outcomes through Wellness and Recovery) in diverse urban and rural community mental health settings. The study compares patient participation and outcomes using the mPOWR system to a usual care control condition. Four community mental health agencies participate in the research: two in San Francisco (urban) and two in N.M. (rural). One site in each setting serves as the mPOWR implementation site and the other serves as the control site. Service sites were randomly assigned to intervention or usual care conditions. A quasi experimental design was used; only eligible participants were enrolled in the study (e.g., exclusion criteria of moderate to severe cognitive impairment, patient services structured for provision of mPOWR implementation, etc.). The study design will employ repeated quantitative measures to assess change in outcomes within and across conditions over time. Qualitative methods in the form of focus group interviews will also be used to round out the information obtained about patient and provider expectations and experiences. Primary outcomes of interest include: Short Form Health Survey-12 (SF-12; physical and mental health aspects of health and well-being); Outcome Rating Scale (ORS; general well-being, personal well-being, close relationships, and work/school/friend relationships); Shared Decision Making Questionnaire (congruence of patient's and provider's participation in therapeutic decision making and patient's understanding of treatment and treatment options); Working Alliance Inventory (perception of therapeutic alliance); and Satisfaction Questionnaire (communication patterns between physicians and their patients).

Eligibility Criteria

Inclusion Criteria

  • Men and women over the age of 18 who are receiving mental health services.

Exclusion Criteria

Temporary Exclusion:

  • Disruptive, aggressive, or severely disorganized behaviors;
  • Visibly intoxicated or under the influence of illicit drugs.

General Exclusion:

  • Moderate to severe cognitive impairment;
  • Developmental disability that precludes comprehension;
  • Language issues: Intervention is only offered in English and Chinese;
  • Patient services structured for provision of mPOWR implementation (e.g., not in and out of inpatient or crisis stabilization services).
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02761733). 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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