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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01353560
Other study ID # 1R01AT005065-01A1-1
Secondary ID 1R01AT005065-01A
Status Completed
Phase N/A
First received May 12, 2011
Last updated June 12, 2017
Start date May 2011
Est. completion date October 2014

Study information

Verified date June 2017
Source Brigham and Women's Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 1509
Est. completion date October 2014
Est. primary completion date October 2014
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 21 Years and older
Eligibility Inclusion Criteria:

- New patient coming into Osher Clinical Center for any medical reason.

- Physician affiliated with any of included division/department (see above).

Exclusion Criteria:

- Patient has been seen at Osher Clinical Center within past 3 months for any reason.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States Osher Clinical Center at Brigham and Women's Hospital Chestnut Hill Massachusetts

Sponsors (3)

Lead Sponsor Collaborator
Brigham and Women's Hospital Beth Israel Deaconess Medical Center, Harvard Medical School

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary 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
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