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Completed

NCT Number: NCT00146679

Psychoeducational Intervention for ICD Patients (PEACE)

The overall purpose of this study is to test the effects of a nurse managed psychoeducational intervention, consisting of symptom management training (SMT) and cognitive-behavioral intervention (CBI), during the first year after ICD implantation using a 3 group randomized clinical trial.

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Key information

Age range

21 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Crawford Long Hospital, Atlanta, Georgia, United States

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About this study

Symptom distress and persistent physical and psychological changes characterize early and ongoing recovery from ventricular dysrhythmia and treatment with an implantable cardiac defibrillator (ICD). This study will test the effect of a psycho educational intervention on psychological and physical outcomes in the first 12 months after ICD implantation. Primary outcome measures are anxiety, depression, and functional status. The effect of the intervention on variables that mediate adaptation and outcomes (symptoms, illness appraisal, and coping behaviors) will also be examined. Secondary aims will examine subsequent arrhythmia events (ICD delivered therapy) and health resource utilization in relation to the main outcomes. The intervention and study variables are based on stress and coping theory and previous research with ICD patients, which documented negative outcomes of ineffective coping and compelling relationships between increased emotional distress and subsequent arrhythmia events.

A three-group, randomized, clinical trial with a repeated-measures design will be used. ICD patients (n=240) will be randomized to receive either the usual standard of care, symptom management training plus cognitive behavioral intervention delivered in a group format, or symptom management training plus cognitive behavioral intervention delivered by nurse provided telephone counseling. The symptom management-training component will be provided in the acute care setting and will focus on symptoms of pain, sleep disturbances and ICD shocks. The four cognitive behavioral sessions by group or telephone format will begin 6-8 weeks after hospitalization and will focus on illness reappraisal and coping skill training. Thus the intervention is designed to bridge the acute and outpatient continuum of care. A booster intervention will be provided at 4 months after implantation. Timeframes for evaluations are baseline, 1, 3, 6, and 12 months after implantation. This study will test whether a cost-effective, accessible, theoretically based, nurse-managed, psycho educational intervention provides an incremental effect over usual care in improving psychological and physical outcomes in ICD patients. This study will provide data upon which future clinical practice guidelines can be based and will establish priorities for patient care according to which interventions are linked to improved adaptive processes and patient outcomes. Greater understanding of the relationships among psychological and physical outcomes, arrhythmia events, and health resource utilization are important for future studies and evaluation of clinical practice with ICD patients.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • All subjects must have a nonthoracotomy insertion
  • Have a primary cardiac etiology of their ventricular arrhythmia (coronary artery disease, cardiomyopathy, valve dysfunction, or combination)
  • Be fluent in English
  • Live within a 75 mile radius of the coordinating center
  • Be accessible by telephone
  • Only those receiving their first ICD, not replacement generators, will be entered.

Exclusion criteria

  • Being evaluated or on a waiting list for heart transplantation
  • Congenital disease or long QT syndrome
  • Disorientation documented in the pre-implantation hospitalization period
  • History of psychiatric disorder or progressively debilitating comorbidity that would confound outcome measures

Treatment and study plan

Psychoeducational Telephone counseling (TC)

Behavioral

Educational and Counseling, symptom management training and cognitive behavioral intervention to teach coping skills provided through telephone sessions

Other names: TC

Psychoeducational Intervention by Group (SG)

Behavioral

Educational and Counseling, symptom management training and cognitive behavioral intervention to teach coping skills provided in 4 group sessions

Other names: SG

Usual Care

Behavioral

Usual Care provided by providers

Other names: UC

Primary outcomes

  1. Anxiety

    Time frame: 3, 6, 12 months

    State-Trait Anxiety Inventory (STAI)

  2. Depression

    Time frame: 3, 6, 12 months

    Beck Depression Inventory II

  3. Functional status

    Time frame: 3, 6, 12 months

    Duke Activity Status Index

Secondary outcomes

  1. Subsequent arrhythmia events documented by ICD therapy

    Time frame: 3, 6, 12 months

    Arrhythmia events log

  2. Patterns of health resource utilization (re-hospitalization, scheduled and unscheduled outpatient visits and contacts, disability days)

    Time frame: 3, 6, 12 months

    Health Resource Use Questionnaire (HRUQ)

  3. Coping

    Time frame: 3, 6 12 months

    Jalowiec Coping Scale

  4. Symptoms

    Time frame: 3,6, 12 months

    Brief Pain Inventory and Pittsburgh Sleep Quality Inventory

Sponsors and collaborators

Lead sponsor

Emory University

Other

Collaborators

  • National Institutes of Health (NIH)

Registry information

Important dates

Study start
2001
Primary completion
2005
Study completion
2006
First posted
Sep 7, 2005
Registry last updated
Sep 10, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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