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Clinical Trials/NCT02643797
NCT02643797
Completed
Phase 3

Medical Assistant Health Coaching for Diabetes in Diverse Primary Care Settings

Scripps Whittier Diabetes Institute1 site in 1 country602 target enrollmentMarch 7, 2016

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Type 2 Diabetes Mellitus (T2DM)
Sponsor
Scripps Whittier Diabetes Institute
Enrollment
602
Locations
1
Primary Endpoint
Glycosylated Hemoglobin (Hba1c); % units
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

This study is a cluster (clinic level) randomized pragmatic trial to compare the effectiveness of MA Health Coaching (MAC) delivered by non-clinician primary care staff (i.e., MAs) versus usual care (UC) in improving diabetes clinical control among individuals with poorly controlled type 2 diabetes mellitus (T2DM).

Detailed Description

The study will be conducted in the primary care environments of two distinct, yet representative healthcare systems in San Diego County: Neighborhood Healthcare (a San Diego County FQHC system and designated Patient-Centered Medical Home, serving predominantly ethnic minority, low income patients) and Scripps (a large, non-profit, private insurance-based health system, serving predominantly Caucasian, middle-to-higher income patients). Six hundred patients at intervention (n=2; patient N=300) and control (n=2; patient N=300) clinics, aged 18 and older, with T2DM, and glycosylated hemoglobin (HbA1c) ≥ 8.0%, and/or low-density lipoprotein cholesterol (LDL-C) ≥ 100 mg/dL, and/or systolic blood pressure (SBP) ≥ 140 within the last 60 days, will be identified and enrolled using electronic health records (EHRs). Primary clinical outcomes of HbA1c, LDL-C, and SBP assessed as part of quarterly (or annual, for LDL-C), standard-of-care medical visits will be extracted from EHRs over 12 months. Changes in patient-reported behavioral (diabetes self-care) and psychosocial (quality of life, patient activation) outcomes will be evaluated via telephone assessment in a subset of intervention and control (N=300 total) participants at baseline, month 6, and month 12. A thorough process evaluation will be conducted to establish reach, acceptability/feasibility, adoption/maintenance, and fidelity of the intervention and will integrate patient, MA, and primary care provider perspectives. Cost-effectiveness will also be examined from the health system perspective. Principles of community engaged research were incorporated in intervention and study planning and will be sustained throughout the research period.

Registry
clinicaltrials.gov
Start Date
March 7, 2016
End Date
April 19, 2020
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Scripps Whittier Diabetes Institute
Responsible Party
Principal Investigator
Principal Investigator

Athena Philis-Tsimikas

Prinicipal Investigator

Scripps Whittier Diabetes Institute

Eligibility Criteria

Inclusion Criteria

  • Must be a patient at selected Scripps or Neighborhood Healthcare clinic,
  • Must be age 18 years or older,
  • Must have a T2DM diagnosis,
  • Must show evidence of poor clinical control, defined as HbA1c ≥ 8% and/or LDL-C ≥ 100 mg/dL, and/or SBP ≥ 140 mmHg.

Exclusion Criteria

  • None as this is a pragmatic trial.

Outcomes

Primary Outcomes

Glycosylated Hemoglobin (Hba1c); % units

Time Frame: 12 months

Systolic blood pressure (SBP); mmHg units

Time Frame: 12 months

Low-density lipoprotein-cholesterol (LDL-c); mg/dL units

Time Frame: 12 months

Secondary Outcomes

  • Summary of Diabetes Self-Care Activities (SDSCA) - patient-reported outcome(12 months)
  • Patient Reported Outcomes Measurement Information System (PROMIS) General Health Scale - patient-reported outcome(12 months)
  • Patient Activation Measure (PAM) - patient-reported outcome(12 months)
  • Patient Assessment of Care for Chronic Conditions (PACIC) - patient-reported outcome(12 months)
  • Morisky Medication Adherence Scale (MMAS) - patient-reported outcome(12 months)

Study Sites (1)

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