IMPACT - Integrative Medicine PrimAry Care Trial

Sponsor
University of Arizona (Other)
Overall Status
Unknown status
CT.gov ID
NCT01785485
Collaborator
(none)
500
1
31.9
15.7

Study Details

Study Description

Brief Summary

This study is Phase II of a project by the University of Arizona Center for Integrative Medicine (AzCIM). Collaborating with AzCIM is the Health Outcomes and Pharmacoeconomics (HOPE) Center and the RAND Corporation, Inc. Phase II is a prospective evaluation of the clinical and cost effectiveness (outcomes) of an integrative medicine professional practice model for adult primary care delivery (the University of Arizona Integrative Health Center - UAIHC in Phoenix, AZ). Data will be gathered from eligible and consenting members of UAIHC. In addition, a fidelity evaluation will assess whether the practice model was implemented as planned.

The specific aims are to: 1) Recruit, consent, and enroll a sample of eligible patient and staff participants from UAIHC; 2) Conduct outcome evaluation of UAIHC care using patient data from medical records abstractions, self-report assessments, clinic administrative and service utilization/encounter data, and health insurance claims data; and, 3) Conduct fidelity evaluation of the implementation of the UAIHC model as described in its business plan using patient- and staff-reported fidelity assessments, random chart audits, and abstracted clinic administrative data.

Participants. 1) Participants from the clinic patient population for whom clinical and cost outcomes will be tracked (n=500); 2) Clinic patients from whom fidelity data will be collected (n=180); and, 3) Clinic personnel from whom fidelity data will also be collected (n=14).

Data Collection. For outcomes evaluation, data will be collected at baseline (initial clinic visit), and at 3-, 6-, and 12-month follow up periods. Sources include clinical symptoms and biomarkers from medical records abstractions; patient reported outcomes and satisfaction questionnaires; clinic service encounter logs; and, cost data from health insurance claims information and clinic financial data. For fidelity evaluation, data will be collected monthly for 6 months after study start, quarterly for the next 6 months, and semi-annually from then on. Patient data for fidelity will be gathered on a single randomized day of the week using a self-administered patient feedback questionnaire. For personnel, fidelity data will be collected at the same intervals using a self-administered provider perceptions questionnaire of inter-professional team and integrative medical care. Data from audits of randomly selected patient charts and administrative records will also be used.

Condition or Disease Intervention/Treatment Phase
  • Other: Integrative medicine primary care model

Study Design

Study Type:
Observational
Anticipated Enrollment :
500 participants
Observational Model:
Case-Control
Time Perspective:
Prospective
Official Title:
IMPACT: Integrative Medicine PrimAry Care Trial: A Comparative Effectiveness Study of an Integrative Primary Care Clinic
Study Start Date :
Feb 1, 2013
Anticipated Primary Completion Date :
Oct 1, 2015
Anticipated Study Completion Date :
Oct 1, 2015

Arms and Interventions

Arm Intervention/Treatment
Primary care patients

Primary care patients who are members of UAIHC.

Other: Integrative medicine primary care model
An integrative medicine primary medical care as defined by the Arizona Center for Integrative Medicine.

Outcome Measures

Primary Outcome Measures

  1. Total healthcare costs from the payer's perspective-total paid costs according to claims data. [12 months of paid costs pre and post beginning membership at UAIHC]

Secondary Outcome Measures

  1. 1. Self-report instruments [Baseline, 3-, 6-, and 12-months]

    Composite: Short Form -12 (Ware, 1996) WHO-5 Well-being Index (Bech, 2003) Perceived Stress Scale (Cohen 1983). Work Productivity and Activity Impairment (Reilly, 1993). Patient Activation Measure (Hibbard, 2004). Diet quality. Behavioral Risk Factor Surveillance System Fruits/Vegetables (CDC, 2012). Physical Activity. Behavioral Risk Factor Surveillance System Physical Activity (CDC, 2012). Stress burden (Littman, 2006). Depression. PHQ-2 (Kroenke, 2003). Anxiety Disorder. GAD-2 (Kroenke, 2007). Pittsburgh Sleep Quality Index (Buysse, 1989). Fatigue visual analogue scale. Fatigue Severity Scale (Krupp, 1989). Pain visual analogue scale. If diagnosed: Fibromyalgia Impact Questionnaire-R (Williams & Arnold, 2011); Roland-Morris Disability Questionnaire (Roland & Morris, 1983); PHQ 9 (Kroenke et al 2002); GAD 7 (Spitzer et al, 2006). Demographics (Baseline). Expectations for care (Baseline). Patient satisfaction. 2-items from the CAHPS (AHRQ, 2012).

  2. Clinical indicators and biomarkers [3-, 6-, and 12-months]

    Composite: Complete metabolic panel, hypoglycemic medication, full lipid panel (TC, HDL, fasting triglycerides), lipid medication, TSH/T4, HbA1c, systolic and diastolic blood pressure, hypertension medication, BMI (height & weight), waist circumference, body fat composition, smoking status, cardiovascular disease risk (general and events), metabolic syndrome diagnosis.

  3. Service Utilization Data and Health Insurance Claims Data [3-, 6-, and 12-months; biennially]

Other Outcome Measures

  1. Patient Experiences (Fidelity) [Monthly for the first 6 mos., then each 3 months for the rest of the first year, then every 6 months.]

    Composite: Dimensions assessed: access to care, whole person care, promotion of self-care and wellness, practitioner communication style, shared decision-making, trust in the practitioner, perceived practitioner empathy, perceived health partnership, and demographic information (CAHPS - AHRQ, 2012; ACES - Safran et al, 1998); CARE - Mercer, et al, 2004).

  2. Provider Experiences (Fidelity) [Monthly for the first 6 months, then each 3 months for the rest of the first year, then every 6 months]

    Composite: Team Climate Inventory Short Version (TCI - Anderson & West, 1995; Loo & Loewen, 2002). Additional items were derived from a study of integrative medicine team practice (Gaboury, et al, 2010). Items on integrative team collaboration, integrative treatment planning, personal development, and clinical skills development were developed for the study.

  3. Medical records chart audit (Fidelity) [Monthly for the first 6 months, then each Monthly first 6 months then q. 3 months for the rest of the first year, then every 6 months]

    Composite: Evidence of principles and best practices of integrative medicine: Whole person assessment and treatment; patient-practitioner health partnership; use of both conventional and CAM methods; health promotion and prevention interventions; use of natural and least invasive treatments where possible (support for body's innate healing capacity); patient personal care support team/team-based approach; extended visits/spending adequate time with patients; access to comprehensive, integrated, care.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Outcomes Study Sample:
Inclusion Criteria:
  • Enrollment in primary care (members) at UAIHC;

  • Adults age 18 or older.

Exclusion Criteria:
  • Currently pregnant at time of recruitment;

  • Patients who attend the UAIHC clinic as consultation-only patients;

  • Significant cognitive impairment to the extent that the individual is unable to understand consent and respond to questionnaires.

Fidelity Study Sample (Patients):
Inclusion Criteria:
  • Enrollment in primary care (members) at UAIHC;

  • Adults age 18 or older.

Exclusion Criteria:
  • Significant cognitive impairment to the extent that the individual is unable to understand consent and respond to questionnaires.
Fidelity Study Sample (Providers):
Inclusion Criteria:
  • All clinical and support personnel.
Exclusion Criteria:
  • None.

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Arizona Integrative Health Center (UAIHC) Phoenix Arizona United States 85012

Sponsors and Collaborators

  • University of Arizona

Investigators

  • Principal Investigator: Victoria Maizes, MD, University of Arizona Arizona Center for Integrative Medicine
  • Study Director: Sally E Dodds, PhD, University of Arizona Arizona Center for Integrative Medicine

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Sally Dodds, Associate Professor/Research Scholar of Medicine & Psychiatry, University of Arizona
ClinicalTrials.gov Identifier:
NCT01785485
Other Study ID Numbers:
  • Coors001
First Posted:
Feb 7, 2013
Last Update Posted:
Feb 7, 2013
Last Verified:
Feb 1, 2013
Keywords provided by Sally Dodds, Associate Professor/Research Scholar of Medicine & Psychiatry, University of Arizona

Study Results

No Results Posted as of Feb 7, 2013