NCT01520662

Brief Summary

Building upon our experience with a very sophisticated preventive services prompt and reminder system, the Preventive Services Reminder System (PSRS), the investigators propose to conduct a systematic three-year study with the following aims:

  1. 1.To develop, field test, and refine an Internet-based patient Wellness Portal linked to PSRS to facilitate patient-centered, preventive care in primary care practices;
  2. 2.To determine the impact of the Wellness Portal on the process of patient-centered preventive care by examining the behavior and experiences of both patients and providers and the degree to which recommended services are individualized; and
  3. 3.To develop model Wellness Portal practices and disseminate the Wellness Portal technology and knowledge derived from Aims 1 and 2 findings.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
540

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Sep 2007

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

September 1, 2007

Completed
10 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2008

Completed
2.1 years until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2010

Completed
1.5 years until next milestone

First Submitted

Initial submission to the registry

January 19, 2012

Completed
11 days until next milestone

First Posted

Study publicly available on registry

January 30, 2012

Completed
Last Updated

January 30, 2012

Status Verified

January 1, 2012

Enrollment Period

10 months

First QC Date

January 19, 2012

Last Update Submit

January 26, 2012

Conditions

Patient-centered Care

Keywords

patient-centered carewellnesspreventive servicesprimary careTo accomplish Aim 2, we will conduct a nine-month pre-postrandomized controlled trial (RCT) in four primary carepractices. The study will focus on the impact of a patientWellness Portal on the quantity and quality of preventivecare patients receive in primary care practices.

Outcome Measures

Primary Outcomes (1)

  • Determine the impact of the Wellness Portal on the process of patient-centered preventive care by examining the experience of patients and providers with care and individualization of recommended services

    9 months run per practice / 12 months total

Secondary Outcomes (1)

  • a) Assess the impact of the Wellness Portal on patient-centered care b) Describe utilization and implementation of the Wellness Portal

    09/01/2007 - 08/31/2010

Study Arms (2)

Wellness Portal Intervention

EXPERIMENTAL

Wellness Portal Intervention: patients have access to the portal in the course of the study.

Other: Implementation of a secure web-based patient Wellness Portal

Wellness Portal Control

NO INTERVENTION

Control patients don't have access to the Wellness Portal in the course of the study.

Interventions

Implementation of a secure web-based patient Wellness PortalOTHER

Patients in intervention practices will review and update their wellness records, risk factor information, allergy and contraindication profile, and personal preferences through the Wellness Portal before they visit their primary care provider.

Wellness Portal Intervention

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • Patients must have been seen at least twice by the enrolled clinician in the last twelve months;
  • Patients must be six years old or younger or 50 years old and older;
  • Patients (or their caretakers) must speak either English or Spanish and must have a basic level of computer skills that include being able to navigate a simple, consumer-oriented web site, use the keyboard and the mouse to interact with the browser, and understand / respond to

You may not qualify if:

  • Not established patient
  • Between than 6 years old and 50 years old
  • Not fluent in English or Spanish, no basic computer skills or no help available for navigating a web browser

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Oklahoma HSC Department of Family and Prevetive Medicne

Oklahoma City, Oklahoma, 73104, United States

Location

Related Links

Study Officials

  • James W Mold, MD, MPH

    University of Oklahoma HSC Department of Family and Preventive Medicine

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
FED
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor, Director of Research Division

Study Record Dates

First Submitted

January 19, 2012

First Posted

January 30, 2012

Study Start

September 1, 2007

Primary Completion

July 1, 2008

Study Completion

August 1, 2010

Last Updated

January 30, 2012

Record last verified: 2012-01

Locations

US(1)