Use and Effectiveness of a Model Integrative Care Clinic in an Academic Hospital: Study 1-Survey
2 other identifiers
observational
1,509
1 country
1
Brief Summary
Despite widespread and growing popularity of complementary and alternative medicine (CAM) in the US, there currently exist significant gaps in our knowledge regarding CAM use, clinical effectiveness, safety and cost- effectiveness. With previous funding support from NCCAM, the Harvard Medical School (HMS) Osher Research Center established and trained a multidisciplinary integrative team of CAM and conventional providers to work collaboratively to provide state-of-the-art "integrative care" in a coordinated and individualized fashion. The Osher Integrative Care Center (OCC) was opened in fall 2007, physically located within the Ambulatory Care Center of the Brigham and Women's Hospital (BWH) at 850 Boylston Street in Chestnut Hill, MA. The focus of this survey study is to characterize the decision-making process of both patients and conventional providers with respect to communication about and referral to an integrative care team in an academic hospital outpatient setting.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started May 2011
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 1, 2011
CompletedFirst Submitted
Initial submission to the registry
May 12, 2011
CompletedFirst Posted
Study publicly available on registry
May 13, 2011
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 1, 2014
CompletedStudy Completion
Last participant's last visit for all outcomes
October 1, 2014
CompletedJune 14, 2017
June 1, 2017
3.4 years
May 12, 2011
June 12, 2017
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Characterization of decision-making process for patients of CAM therapies and conventional providers
Surveys will be sent to: 1) 1500 consecutive new patients seen at the OCC over 3.5 years, to characterize the chief complaints; their medical history; referral sources; communication with their physicians; barriers to use of CAM; views regarding and previous use of CAM; and expectations for CAM therapy as adjuncts to their conventional care; 2) 300 BWH physicians from five divisions (Women's Health, Orthopedics, Obstetrics and Gynecology, General Medicine, and Rheumatology) most likely to refer to the OCC, to assess their use of, feelings about, and knowledge of CAM.
3.5 years
Study Arms (1)
New patients of Osher Clinical Center
Eligibility Criteria
1. All new patients coming into the Osher Clinical Center (OCC) for any medical reason. 2. All physicians in the 5 included departments/divisions (Women's Health, Orthopedics, Obstetrics and Gynecology, General Medicine, and Rheumatology) are eligible to participate in the survey. Other BWH physicians whom OCC patients have identified as their referring doctors and given us permission to contact, will also be eligible to participate in the survey.
You may qualify if:
- New patient coming into Osher Clinical Center for any medical reason.
- Physician affiliated with any of included division/department (see above).
You may not qualify if:
- Patient has been seen at Osher Clinical Center within past 3 months for any reason.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Brigham and Women's Hospitallead
- Harvard Medical School (HMS and HSDM)collaborator
- Beth Israel Deaconess Medical Centercollaborator
Study Sites (1)
Osher Clinical Center at Brigham and Women's Hospital
Chestnut Hill, Massachusetts, 02467, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Julie E Buring, ScD
Brigham and Women's Hospital
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
May 12, 2011
First Posted
May 13, 2011
Study Start
May 1, 2011
Primary Completion
October 1, 2014
Study Completion
October 1, 2014
Last Updated
June 14, 2017
Record last verified: 2017-06