Functional Assessment Screening Tablets - Patient Reported Measures

This study has been completed.
Sponsor:
Collaborator:
RAND
Information provided by (Responsible Party):
Rachel Hess, University of Pittsburgh
ClinicalTrials.gov Identifier:
NCT01080183
First received: February 27, 2010
Last updated: September 9, 2011
Last verified: September 2011

February 27, 2010
September 9, 2011
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. ] [ Designated as safety issue: Yes ]
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
Not Provided
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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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Interventional
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Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Single Blind (Outcomes Assessor)
Primary Purpose: Health Services Research
Smoking
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
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
150
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.
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT01080183
PRO09080140
No
Rachel Hess, University of Pittsburgh
University of Pittsburgh
RAND
Principal Investigator: Rachel Hess, MD University of Pittsburgh
University of Pittsburgh
September 2011

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