The Effect of Action Control Based Intervention on Adherence After Cardiac Rehabilitaiton

This study has been completed.
Sponsor:
Information provided by:
Summa Health System
ClinicalTrials.gov Identifier:
NCT00602485
First received: January 15, 2008
Last updated: September 17, 2009
Last verified: September 2009
  Purpose

This will be a pilot study of the effect of an Action Control-based intervention (ACBI) on adherence to prescribed diet and exercise programs after cardaic rehabilitation. The purposes of this study are to:

  1. determine if an ACBI has an effect on adherence to prescribed home exercise and diet regimens for individuals 6 weeks after participating in a cardiac rehabilitation program
  2. examine whether there is a difference in response to the ACBI between state-oriented individuals and action-oriented individuals.
  3. test the interaction effect between action-orientation disposition and the intervention.

Condition Intervention Phase
Heart Failure
Other: Action Control Education
Phase 1

Study Type: Interventional
Study Design: Allocation: Non-Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Prevention
Official Title: The Effect of Action Control Based Interventions on Adherence to Prescribed Exercise and Diet Regimens for Patients Completing a Cardiac Rehabilitation Program Intervetnion on

Resource links provided by NLM:


Further study details as provided by Summa Health System:

Primary Outcome Measures:
  • self-report adherence to exercise and diet prescriptions [ Time Frame: 6 weeks post cardaic rehabilitation ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • action control orientaiton based on adherence [ Time Frame: 6 weeks post cardaic rehabilitaiotn ] [ Designated as safety issue: No ]

Estimated Enrollment: 80
Study Start Date: June 2007
Study Completion Date: February 2009
Primary Completion Date: February 2009 (Final data collection date for primary outcome measure)
Intervention Details:
    Other: Action Control Education
    30 minute educational intervnetion
Detailed Description:

Patients with cardiac problems are burdened with complex lifestyle changes involving medication, diet and exercise. Non-adherence to prescribed treatment protocols is a major contributor to morbidity and mortality for these indiviudals. Rehabbilitation programs provide the necessary education and supervision needed to promote health, however, non-adherence occurs even for those indiviudals with appropriate resources and motivation. Most of the research up to this point deals with preparing indiviudals to be adherent. Action Control theory is focused on the mental processes that occur between the time an individual makes a decision to adhere and the moment when the appropriate activty either occurs or does not occur.

This interventions tudy will compare rates of adherece between indivudals who receive an action control based educational intervention and those who do not.

  Eligibility

Ages Eligible for Study:   21 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Participants will be a convenience sample of English literate men and women over the age of 21 enrolled in a cardiac rehabilitation program and accessible by phone for follow-up. All participants are referred to rehabilitation by their physician. Being enrolled in the program indicates the participants have experienced a serious cardiac event, either myocardial infarction and/or coronary surgery

Exclusion Criteria:

  • Non-English literate, uner teh age of 21
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00602485

Locations
United States, Ohio
Summa Health System
Akron, Ohio, United States, 44309
Sponsors and Collaborators
Summa Health System
Investigators
Principal Investigator: Carrie J Scotto, PhD Summa Health System
  More Information

No publications provided

Responsible Party: Donna Waechter, Ph.D., Summa Health System
ClinicalTrials.gov Identifier: NCT00602485     History of Changes
Other Study ID Numbers: R07026
Study First Received: January 15, 2008
Last Updated: September 17, 2009
Health Authority: United States: Institutional Review Board

Keywords provided by Summa Health System:
adherence, cardiac rehabilitation

Additional relevant MeSH terms:
Heart Failure
Heart Diseases
Cardiovascular Diseases

ClinicalTrials.gov processed this record on July 23, 2014