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

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00602485
First Posted: January 28, 2008
Last Update Posted: September 18, 2009
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
Summa Health System
  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
Intervention Model: Single Group Assignment
Masking: None (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 ]

Secondary Outcome Measures:
  • action control orientaiton based on adherence [ Time Frame: 6 weeks post cardaic rehabilitaiotn ]

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

Information from the National Library of Medicine

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Ages Eligible for Study:   21 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
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
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): 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

Responsible Party: Donna Waechter, Ph.D., Summa Health System
ClinicalTrials.gov Identifier: NCT00602485     History of Changes
Other Study ID Numbers: R07026
First Submitted: January 15, 2008
First Posted: January 28, 2008
Last Update Posted: September 18, 2009
Last Verified: September 2009

Keywords provided by Summa Health System:
adherence, cardiac rehabilitation

Additional relevant MeSH terms:
Heart Failure
Heart Diseases
Cardiovascular Diseases