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Clinical Trials/NCT04899752
NCT04899752CompletedNot Applicable

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

Auburn University2 sites in 1 country89 target enrollmentStarted: June 1, 2021Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
89
Locations
2
Primary Endpoint
Dartmouth Quality of Life index

Study Overview

Brief 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.

Detailed 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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Participant)

Masking Description

Participants will not be award of group assignments as all participants are provided a face-to-face interaction with the provider.

Eligibility Criteria

Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Enrolled in outpatient cardiac rehab
  • Able to complete the paperwork independently

Exclusion Criteria

  • Unable to complete assessments and paperwork independently.

Outcomes

Primary Outcomes

Dartmouth Quality of Life index

Time Frame: 12 weeks

Changes in Dartmouth Quality of Life Index. Range is 9-45. Higher score indicates lower quality of life.

6-minute walk

Time Frame: 12 weeks

Changes in the distance traveled during a 6-minute walk

Adherence to CR

Time Frame: 12 weeks

Differences in the number of sessions attended between groups

Rate my plate

Time Frame: 12 weeks

Changes in heart healthy diet

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Danielle D Wadsworth

Associate Professor

Auburn University

Study Sites (2)

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