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Functional Assessment Screening Tablets - Patient Reported Measures

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University of Pittsburgh

Status

Completed

Conditions

Smoking

Treatments

Other: Patient feedback form

Study type

Interventional

Funder types

Other

Identifiers

NCT01080183
PRO09080140

Details and patient eligibility

About

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.

Enrollment

150 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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.

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

150 participants in 2 patient groups

Feedback form
Experimental group
Description:
patients receive feedback regarding their prms in addition to doctor receiving report
Treatment:
Other: Patient feedback form
usual care
No Intervention group
Description:
patients do not receive feedback form prior to the encounter, clinicians continue to receive patient reported measures prior to the appointment

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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