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Motivational Interviewing & Clinician Centered Interviewing on Cardiac Rehab

NCT ID: NCT04899752

Last Updated: 2022-12-23

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

89 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-06-01

Study Completion Date

2022-12-01

Brief Summary

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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

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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.

Conditions

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Cardiac Rehabilitation Motivational Interviewing

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Participants are randomly assigned to one of three groups.
Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

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

Study Groups

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Traditional OPCR

Those who are in the traditional group will discuss topics like medication adherence, physical activity questions, or eating habits without a clear from of autonomy or nonautonomy basis as is currently completed in OPCR. This will occur in a face to face format.

Group Type EXPERIMENTAL

Motivational Interviewing

Intervention Type BEHAVIORAL

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

OPCR + MI

The MI group will be consistent with the spirit of MI and utilize a high autonomy communication style to provide support for behavior change across multiple behaviors. This will occur in a face to face format.

Group Type EXPERIMENTAL

Motivational Interviewing

Intervention Type BEHAVIORAL

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

OPCR + Clinician centered

The OPCR + CC group will participate in low-autonomy face to face interviews. Meaning the communication style will be clinician centered, providing goals to the participants without valuing their input.

Group Type EXPERIMENTAL

Motivational Interviewing

Intervention Type BEHAVIORAL

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

Interventions

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Motivational Interviewing

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

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

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

Exclusion Criteria

* Unable to complete assessments and paperwork independently.
Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Auburn University

OTHER

Sponsor Role lead

Responsible Party

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Danielle D Wadsworth

Associate Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Danielle D Wadsworth, PhD

Role: PRINCIPAL_INVESTIGATOR

Auburn University

Locations

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Auburn University

Auburn, Alabama, United States

Site Status

Countries

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United States

Other Identifiers

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20-512 EP 2011

Identifier Type: -

Identifier Source: org_study_id