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HEART Camp: Promoting Adherence to Exercise in Patients With Heart Failure

NCT01658670 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 245

Last updated 2023-11-09

No results posted yet for this study

Summary

The purpose of this study is to determine the efficacy of the Heart Failure Exercise and Resistance Training (HEART) Camp behavioral exercise training intervention on long-term adherence to exercise at 18 months in patients with heart failure. The central hypothesis is that the HEART Camp intervention group (HC) will have significantly better adherence to exercise at 18 months.

Conditions

Interventions

BEHAVIORAL

Enhanced Usual Care Group

The EUC group is provided access to the exercise facility and regular facility staff for the 18 month study period.

BEHAVIORAL

HEART Camp (HC) Intervention Group

The HC intervention group will be provided access to the exercise facility for the 18 month study period and will also receive the cognitive-behavioral intervention (knowledge, attitudes, self-efficacy, behavioral self-management skills and social support) delivered using both group-based and individual-based strategies.

Sponsors & Collaborators

  • National Heart, Lung, and Blood Institute (NHLBI)

    collaborator NIH

  • Wayne State University

    collaborator OTHER

  • Henry Ford Health System

    collaborator OTHER

  • University of Nebraska Lincoln

    collaborator OTHER

  • University of Nebraska

    lead OTHER

Principal Investigators

  • Bunny J Pozehl, PhD, RN · University of Nebraska

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
19 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-04-01
Primary Completion
2016-12-01
Completion
2018-03-01

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01658670 on ClinicalTrials.gov