Impact of a Wellness Portal on The Delivery of Patient-Centered Preventive

Status Completed

Clinical Trial 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. 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. 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. To develop model Wellness Portal practices and disseminate the Wellness Portal technology and knowledge derived from Aims 1 and 2 findings.

Clinical Trial Description

Project Aim 1: Develop, field test, and further refine an Internet-based Wellness Portal for use by patients seen in primary care settings to facilitate patient-centered, preventive care.

Specific Objectives:

- Assemble an Advisory Committee of clinicians, office staff, patients, and national HIT experts and develop a patient Wellness Portal that can be accessed by patients through the Internet and also in the provider's office via computer kiosks;

- Field test the Wellness Portal in two OKPRN practices and collect patient and provider satisfaction data via surveys and personal feedback to improve and refine the Wellness Portal and its integration into the comprehensive care delivery process.

Project Aim 2: 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.

Specific Objectives:

- Assess the impact of the Wellness Portal on patient-centered care:

1. Assess the impact of the Wellness Portal on patient activation and the medical home;

2. Understand the impact of Wellness Portal use, the role of activated patients, and the concept of medical home on the provision of patient-centered care;

3. Measure the impact of the Wellness Portal on the individualization of preventive services that are recommended and delivered based upon individual risk factors and patient preferences;

- Describe utilization and implementation of the Wellness Portal, capture and analyze documented decisions on opting out from evidence-based recommendations, and assess the impact of the portal on missed opportunities for delivering preventive care. ;

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention

Related Conditions & MeSH terms

Patient-centered Care

Clinical Trial Details

NCT number	NCT01520662
Study type	Interventional
Source	Agency for Healthcare Research and Quality (AHRQ)
Contact
Status	Completed
Phase	N/A
Start date	September 2007
Completion date	August 2010

View Details

See also
Status	Clinical Trial	Phase
Completed	`NCT03283891` - Effects on Nurses' Quality of Working Life of an Educational Intervention to Strengthen Their Humanistic Practice	N/A
Completed	`NCT03722017` - Drug Reduction in Older Patients: The DROP Trial	N/A
Completed	`NCT02870296` - Anticoagulation Medical Home	N/A
Completed	`NCT06239987` - The Effect of Care-oriented Practical Training on Nurses' Intensive and Critical Care Competency and HAIs Indicators	N/A
Completed	`NCT03097640` - Understanding Perspectives of Frequently-Admitted Hospital Patients	N/A
Recruiting	`NCT05906888` - Weaning With Tracheostomy - an Observational Study on Patient-centered Outcomes
Recruiting	`NCT05424809` - Feasibility and Preliminary Effectiveness of a Shared Decision-making Process	N/A
Completed	`NCT01542112` - An Innovational Model to Manage Patient Expectations and Improve Patient Satisfaction: An Intervention Study	N/A
Completed	`NCT01575990` - Elders Preferences in Care Decisions	N/A
Completed	`NCT03503487` - Surgical Planning and Informed Consent	N/A
Recruiting	`NCT05659485` - Measuring Family Engagement in Care (The FAME Study)
Active, not recruiting	`NCT06187428` - The PainSMART Research Program: Evaluating a Pain Education Strategy for Patients Seeking Primary Care Physiotherapy	N/A
Completed	`NCT03182283` - Person-Centered Psychosis Care: An Educational Intervention	N/A

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

Impact of a Wellness Portal on The Delivery of Patient-Centered Preventive Care

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms