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CompletedNCT00602485Updated Sep 18, 2009

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

A Phase 1 interventional study of Action Control Education in Heart Failure, sponsored by Summa Health System. Completed at 1 site in United States. Open to participants aged 21 Years and older. Per ClinicalTrials.gov, last updated 2009-09-18.

Sponsored by Summa Health System · Phase 1, Interventional, and Prevention

Phase
Phase 1
Study type
Interventional
Enrollment
80
Allocation
Non-randomized
Ages
21 Years and older
Sex
All
01

Study summary

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.
Read the 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.

02

Conditions studied

  • Heart Failure

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Keywords

  • adherence, cardiac rehabilitation
03

In context

Heart Failure

5,803 studies on the registry are indexed under Heart Failure; 1,222 are open to participants now.

This study's planned enrollment of 80 is above the median of 72 across 3,790 interventional studies indexed under Heart Failure.

Browse Heart Failure studies →

Lead sponsor

Summa Health System is the lead sponsor of 20 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
21 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

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

Exclusion Criteria:

  • Non-English literate, uner teh age of 21
05

Study design

Phase
Phase 1
Primary purpose
Prevention
Allocation
Non-randomized
Intervention model
Single group
Masking
None (open label)
Enrollment
80 participants (estimated)

Interventions

  • OtherAction Control Education

    30 minute educational intervnetion

06

What researchers measure

Primary outcomes

  1. self-report adherence to exercise and diet prescriptions

    Time frame: 6 weeks post cardaic rehabilitation

Secondary outcomes

  1. action control orientaiton based on adherence

    Time frame: 6 weeks post cardaic rehabilitaiotn

07

Study locations

1 site
  • Summa Health System
    Akron, Ohio 44309, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 18, 2009, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00602485
Lead sponsor
Summa Health System
First posted
Jan 28, 2008
Start date
Jun 2007
Primary completion
Feb 2009
Completion
Feb 2009
Last update
Sep 18, 2009

Study contacts

Carrie J Scotto, PhD
principal investigator · Summa Health System

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Sep 2009. You cannot join it, but the record below documents what was studied.

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