Functional Assessment Screening Tablets - Patient Reported Measures

Smoking Clinical Trial

Official title:

Functional Assessment Screening Tablets - Patient Reported Measures Translating Research Into Practice Pilot

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01080183
• Other study ID #: PRO09080140
• Status: Completed
• Phase: N/A
• First received: February 27, 2010
• Last updated: January 13, 2016
• Start date: March 2010
• Est. completion date: October 2010

Study information

• Verified date: January 2016
• Source: University of Pittsburgh
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Interventional

Clinical Trial Summary

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 150
• Est. completion date: October 2010
• Est. primary completion date: October 2010
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

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.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Health Services Research

Related Conditions & MeSH terms

• Smoking

Intervention

Other:
• Patient feedback form
patients receive a report that feeds back their patient reported measures to them prior to their clinical visit

Locations

Country	Name	City	State
United States	General Internal Medicine Oakland	Pittsburgh	Pennsylvania

Sponsors (2)

Lead Sponsor	Collaborator
University of Pittsburgh	RAND

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Doctor Patient Communication	the doctor patient and encounter will be queried for communication regarding the patient reported measures	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.	Yes