Motivational Interviewing & Clinician Centered Interviewing on Cardiac Rehab

Cardiac Rehabilitation Clinical Trial

— MIOPCR  

Official title:

The Effect of Motivational Interviewing and Clinician Centered Interviewing Based Cardiac Rehabilitation on Core Outcomes

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04899752
• Other study ID #: 20-512 EP 2011
• Status: Completed
• Phase: N/A
• Start date: June 1, 2021
• Est. completion date: December 1, 2022

Study information

• Verified date: December 2022
• Source: Auburn University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this project is to examine the differences in outpatient cardiac rehab (OPCR) core component outcomes on different intervention conditions. Conditions include traditional OPCR (control), OPCR + motivational interviewing (MI) and OPCR + Clinician centered interviews.

Description:

Participants who are beginning a OPCR program at a local hospital are eligible for the program. During the standard admission procedures, eligible participants will be provided with a consent from and asked to participate in the study. Participants who provide consent will complete their admission packet. The standard admission packet includes: the Outpatient Fall Assessment Risk, Patient Health Questionnaire (PHQ-9),the Dartmouth Quality of Life, and the Rate Your Plate. In addition participants will complete three additional surveys: the Intrinsic Motivation Inventory (IMI), the FPS, (FACES Pain Scale), and the Brief Resilience Scale (BRS). During their second appointment participants will complete the standard 6 minute walk test which is scheduled at their convenience and the grip strength. Participants will then be randomly assigned to the traditional OPCR, the OPCR + MI, or the OPCR - Clinician centered. Post-testing will include all baseline information as well as information from patients charts (lipid profile, HbA1c, risk factors and family history). Analysis will determine differences in core outcomes between the three groups.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 89
• Est. completion date: December 1, 2022
• Est. primary completion date: March 31, 2022
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: N/A and older

Eligibility

Inclusion Criteria:

• Enrolled in outpatient cardiac rehab

• Able to complete the paperwork independently

Exclusion Criteria:

• Unable to complete assessments and paperwork independently.

Related Conditions & MeSH terms

• Cardiac Rehabilitation
• Motivational Interviewing

Intervention

Behavioral:
• Motivational Interviewing
Participants will participate in three different communication styles to determine the effect of MI on cardiac rehab outcome measures.

Locations

Country	Name	City	State
United States	Auburn University	Auburn	Alabama

Sponsors (1)

Lead Sponsor	Collaborator
Auburn University

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Adherence to CR	Differences in the number of sessions attended between groups	12 weeks
Primary	6-minute walk	Changes in the distance traveled during a 6-minute walk	12 weeks
Primary	Rate my plate	Changes in heart healthy diet	12 weeks
Primary	Dartmouth Quality of Life index	Changes in Dartmouth Quality of Life Index. Range is 9-45. Higher score indicates lower quality of life.	12 weeks