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Functional Assessment Screening Tablets - Patient Reported Measures

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
ClinicalTrials.gov Identifier: NCT01080183
Recruitment Status : Completed
First Posted : March 3, 2010
Last Update Posted : January 15, 2016
Information provided by (Responsible Party):

February 27, 2010
March 3, 2010
January 15, 2016
March 2010
October 2010   (Final data collection date for primary outcome measure)
Doctor Patient Communication [ Time Frame: The doctor and patient pair will complete a one time survey within two weeks of the doctor patient encounter. Audiotaping of the encounter will occur once at the time of encounter. ]
the doctor patient and encounter will be queried for communication regarding the patient reported measures
Same as current
Complete list of historical versions of study NCT01080183 on ClinicalTrials.gov Archive Site
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Functional Assessment Screening Tablets - Patient Reported Measures
Functional Assessment Screening Tablets - Patient Reported Measures Translating Research Into Practice Pilot
The team's ultimate goal is to improve health care quality and effectiveness and support patient-centered care. In this project, we, the investigators, will test whether providing patients with guideline based-recommendations regarding tobacco use, physical activity and mental and physical health-related quality of life (patient reported measures: PRMs) using health information technology increases doctor-patient discussions regarding these topics and results in improvements in PRMs. We will randomize physicians in a single general internal medicine practice. Patients seeing intervention physicians will receive guideline-based recommendations regarding PRMs, those seeing control physicians will not. We will compare differences in doctor-patient discussions regarding PRMs between the intervention and control groups. The successful completion of this project will provide evidence the effectiveness of involving patients in their care through the use guideline-based feedback.
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Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Outcomes Assessor)
Primary Purpose: Health Services Research
Other: Patient feedback form
patients receive a report that feeds back their patient reported measures to them prior to their clinical visit
  • Experimental: Feedback form
    patients receive feedback regarding their prms in addition to doctor receiving report
    Intervention: Other: Patient feedback form
  • No Intervention: usual care
    patients do not receive feedback form prior to the encounter, clinicians continue to receive patient reported measures prior to the appointment
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
October 2010
October 2010   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • physicians who see patients in the University of Pittsburgh General Internal Medicine Practice.
  • patients of physician's who have consented to participate.

Exclusion Criteria:

  • age less than 18.
Sexes Eligible for Study: All
18 Years and older   (Adult, Senior)
Contact information is only displayed when the study is recruiting subjects
United States
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Rachel Hess, University of Pittsburgh
University of Pittsburgh
Principal Investigator: Rachel Hess, MD University of Pittsburgh
University of Pittsburgh
January 2016

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP