Reducing Risk in Cardiac Rehabilitation: Partners Together in Health (PaTH) Intervention Study

NCT ID: NCT00926848

Last Updated: 2023-09-25

Study Results

Results available

Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.

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Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

68 participants

Study Classification

INTERVENTIONAL

Study Start Date

2009-07-01

Study Completion Date

2012-06-01

Brief Summary

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The objective of the proposed study, using an experimental, two-group (n = 30 couples in each group) repeated measures design, was to pilot test the effects of the PaTH Intervention versus a usual care group in improving the following outcomes: a) physical activity and healthy eating behaviors, and b) functional capacity. The primary outcomes will be physical activity behavior (minutes per week) and eating behavior (percent saturated fat) at the 6 month time point in both the coronary artery bypass graft (CABG) patient and his/her partner. Secondary outcome includes functional capacity in patients and partners at 6 months.

Detailed Description

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Long-term maintenance of lifestyle changes to reduce cardiovascular risk factors after coronary artery bypass graft (CABG) surgery is essential to positively influence health outcomes. Despite proven efficacy of cardiac rehabilitation (CR) in helping patients initiate lifestyle changes, less than 50% of CABG patients maintain lifestyle changes by 6 months post-CABG. It is known that the spouse is the main source of social support for the recovering cardiac patient and frequently attends cardiac rehabilitation with the patient to provide transportation, emotional support, or attend educational classes. In spite of these supportive behaviors, however; adherence still drops off after CR. Lifestyle interventions that specifically target the marital partners as a unit may be more efficacious than current individually-oriented education strategies. The objective of the proposed feasibility study, using an experimental, two-group (n = 30 couples in each group) repeated measures design, will be to pilot test the effects of the Partners Together in Health (PaTH) Intervention versus usual care in improving physical activity and healthy eating behaviors, and functional capacity. The specific aims are to assess the feasibility of implementing the PaTH Intervention and generate pilot data on all outcome variables in both the CABG patient and the partner to estimate effect sizes needed to determine the sample size requirements for the larger study. Partners in the PaTH Intervention group will formally join CR with the patient to participate in exercise sessions and educational classes to undertake comprehensive risk reduction for themselves, and to make the same positive physical activity/exercise and healthy eating lifestyle changes as the patient. Partners in the usual care group will be invited to attend the educational sessions with the patient as is currently usual care. The primary outcomes will be physical activity behavior (minutes per week) and eating behavior (percent saturated fat) at the 6 month time point in both the coronary artery bypass graft (CABG) patient and his/her partner. The secondary outcome includes functional capacity in patients and partners at 6 months. The PaTH intervention is innovative because it allows the couple to build new habits together so they can motivate and support one another on their journey toward health, it uses an existing, well-established treatment method (cardiac rehab) to deliver cost-effective care (Balady et al., 2007), it provides self-efficacy and social support for both members of the dyad in making behavioral changes, and no other studies testing the effects of including the partner in CR were found.

Conditions

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Coronary Heart Disease Cardiac Rehabilitation

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Patients and partners in the PaTH intervention group formally joined and participated in the full cardiac rehabilitation (CR) program consisting of 18-36 exercise and 18 educational sessions. In the usual care group, only patients received the exercise and educational sessions; partners received the educational sessions only.
Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors
The research personnel who were collecting outcomes data were unaware of the subjects' group assignment.

Study Groups

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PaTH intervention group

The PaTH intervention group for patients and partners consisted of participation in a structured and formal cardiac rehabilitation program:

* 18-36 exercise sessions
* 18 educational sessions. The intervention consisted of patients and partners participating together in a formal cardiac rehabilitation program when typically just patients participate. In addition, partners were asked to make the same healthy eating and exercise changes that patients did to meet guidelines for health.

Group Type EXPERIMENTAL

Partners Together in Health (PaTH) Intervention

Intervention Type BEHAVIORAL

Patients and partners in the PaTH experimental group participated in 18-36 exercise and 18 educational sessions in a structured cardiac rehabilitation program. Patients in the Usual care group also participated in 18-36 exercise and 18 educational sessions; partners, however, only participated in the educational sessions.

Usual care group

The usual care group intervention for patients only consisted of participation in a structured and formal cardiac rehabilitation program:

* 18-36 exercise sessions and 18 educational sessions

Partners participated in the 18 educational sessions only.

Group Type ACTIVE_COMPARATOR

Partners Together in Health (PaTH) Intervention

Intervention Type BEHAVIORAL

Patients and partners in the PaTH experimental group participated in 18-36 exercise and 18 educational sessions in a structured cardiac rehabilitation program. Patients in the Usual care group also participated in 18-36 exercise and 18 educational sessions; partners, however, only participated in the educational sessions.

Interventions

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Partners Together in Health (PaTH) Intervention

Patients and partners in the PaTH experimental group participated in 18-36 exercise and 18 educational sessions in a structured cardiac rehabilitation program. Patients in the Usual care group also participated in 18-36 exercise and 18 educational sessions; partners, however, only participated in the educational sessions.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* age 19 or older
* diagnosis of first-time coronary artery bypass graft surgery (CABGs) and enrollment in outpatient CR
* married or living with partner for more than 1 year
* partner is also willing to participate
* no history of psychiatric illness
* classified as low to moderate risk for the occurrence of cardiac events during exercise (AACVPR, 2004).
* first-time CABG patients

Eligible partners will:

* be age 19 or older
* have no history of psychiatric illness
* be classified as low to moderate risk for the occurrence of cardiac events during exercise
* have written permission from the partner's primary health care provider to participate in the study.

Exclusion Criteria

* orthopedic problems that would prevent them from walking or exercising
* history of cardiac arrest, sudden death, complex dysrhythmias at rest, or CHF diagnosis
* resting systolic BP \> 200 mmHg or diastolic BP \> 100 mmHg
* a concomitant diagnosis or procedure such as valve repair/replacement or aneurysmectomy
* debilitating non-cardiac disease such as renal failure or anemia
* severe chronic obstructive lung disease (FEV1 \< 1 liter)
* poorly controlled diabetics (diagnosed with diabetic ketoacidosis within the past 6 months or a current HgA1c \> 11).
Minimum Eligible Age

19 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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National Institute of Nursing Research (NINR)

NIH

Sponsor Role collaborator

University of Nebraska

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Bernice C Yates, PhD

Role: PRINCIPAL_INVESTIGATOR

University of Nebraska

Locations

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University of Nebraska Medical Center

Omaha, Nebraska, United States

Site Status

Countries

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United States

Other Identifiers

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1R15NR010923-01A1

Identifier Type: NIH

Identifier Source: secondary_id

View Link

0544-08-FB

Identifier Type: -

Identifier Source: org_study_id

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