Effects of a Hybrid Model of Cardiac Rehabilitation on Patient Outcomes

NCT ID: NCT06030115

Last Updated: 2023-09-08

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

Total Enrollment

100 participants

Study Classification

OBSERVATIONAL

Study Start Date

2019-07-01

Study Completion Date

2021-07-31

Brief Summary

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Determine if the standard of care at a cardiac rehabilitation center using what the investigators term to be "hybrid model" on the exercise component of cardiac rehabilitation is associated with improved adherence and outcomes. Discuss the hybrid model in comparison to traditional cardiac rehabilitation and layout a template on how to incorporate this hybrid model. Discuss factors that may lead to poor adherence and attendance to cardiac rehabilitation.

Detailed Description

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Purpose: The aim of this prospective cohort study was to determine the effectiveness of an individualized physical therapist (PT) driven hybrid model of the exercise component of cardiac rehabilitation (CR) that uses a novel intensity-recovery progression protocol (IRPP) and cardiac testing template (CTT) to assess achieved heart rate intensity (AHRI%), heart rate recovery (HRR%), and intensity-recovery total (IR%) as indicators to guide treatment.

Methods: Assessment of a subjective questionnaire, vital signs, treadmill 6-minute walk (6MW), 1-minute sit-to-stand (1STS), 1-minute step (1ST), and 1-minute agility square tests (1AST) were assessed on 100 participants during the 36-visit program. The hybrid model was led by a PT, was longer in duration, added high intensity interval training (HIIT) to continuous aerobic exercise training (CAET) and resistance training, and used a 1:1 treatment ratio. Treatment intensity and progression were measured based on clinical decision making through the IRPP and CTT.

Conditions

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Cardiac Surgery Coronary Artery Bypass Graft CABG Stent Valve Replacement

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Cardiac Rehab Patients

All participants referred to the clinic meeting the inclusion and exclusion criteria who wanted to participate in the study.

Exercise Component Of Cardiac Rehabilitation (Hybrid Model) Intensity Recovery Progression Protocol (IRPP)

Intervention Type OTHER

Data collected on participants who completed the intensity recovery progression protocol program

Interventions

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Exercise Component Of Cardiac Rehabilitation (Hybrid Model) Intensity Recovery Progression Protocol (IRPP)

Data collected on participants who completed the intensity recovery progression protocol program

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Underwent cardiac surgery (CABG, PCI with stent placement, and valve replacement)
* Surgery was within the previous 365 days
* Could independently ambulate into the facility.

* Diagnosed a-fib
* Participants who attended cardiac rehabilitation before

Exclusion Criteria

* Implantable cardioverter defibrillator (ICD)
* Pacemaker (PPM)
* Heart Transplant
* Left ventricular assist device (LVAD)
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Good Shepherd Integrated Healthcare Systems

OTHER

Sponsor Role lead

Responsible Party

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Kevin Minchin

Physical Therapist, Rehabilitation Director

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Kevin Minchin, DPT

Role: PRINCIPAL_INVESTIGATOR

Good Shepherd

Locations

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Good Shepherd Integrated Healthcare Systems

Las Vegas, Nevada, United States

Site Status

Countries

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United States

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Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

GoodShepherdIHS

Identifier Type: -

Identifier Source: org_study_id

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