Effect of Peer Support Intervention on Early Recovery Outcomes Post Coronary Artery Bypass Graft Surgery

Sponsor
University of Calgary (Other)
Overall Status
Completed
CT.gov ID
NCT01775228
Collaborator
Heart and Stroke Foundation of Canada (Other), Canadian Council of Cardiovascular Nurses (Other)
185
3
2
36
61.7
1.7

Study Details

Study Description

Brief Summary

Recovery from coronary artery bypass graft (CABG) surgery is a complex process involving physical recuperation and psychological adjustment. The high prevalence of postoperative depression in this population may threaten optimal recovery. Peer support over the recovery period has promise to mitigate this threat. The purpose of this study was to examine the effect of a professionally-guided telephone peer support intervention on recovery outcomes including depression, social support and health care resource utilization.

In a randomized controlled trial, 185 male CABG surgery patients randomly assigned to an intervention (n=61) or usual care (n=124) group. Participants in the intervention group received weekly telephone calls from a peer volunteer over 6 weeks post discharge. At hospital discharge and at 6 and 12 weeks follow up, depression was measured using the Beck Depression Scale-II, social support was measured using the Shortened Social Support Scale and health care resource utilization was measured using items in the Postoperative Self Report of Recovery Questionnaire. Participants in the intervention group were also asked questions about their perceptions regarding peer support using the Peer Support Evaluation Inventory.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Peer Support
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
185 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Official Title:
The Effect of a Professionally-guided Telephone Peer Support Intervention on
Study Start Date :
Nov 1, 2006
Actual Primary Completion Date :
Nov 1, 2008
Actual Study Completion Date :
Nov 1, 2009

Arms and Interventions

Arm Intervention/Treatment
No Intervention: Regular follow up care

No intervention group - received routine follow up care following discharge from hospital after cardiac surgery (no peer support intervention).

Active Comparator: Peer Support intervention

Support (informational, emotional and appraisal) in the form of like persons (i.e. age, gender) who have undergone CABG surgery with successful outcomes (post-recovery at least one year); peer support was provided by telephone for 6 weeks post cardiac surgery recovery.

Behavioral: Peer Support
Support (informational, emotional and appraisal) in the form of like persons (i.e. age, gender) who have undergone CABG surgery with successful outcomes (post-recovery at least one year); peer support was provided by telephone for 6 weeks post cardiac surgery recovery.
Other Names:
  • Social Support
  • Outcome Measures

    Primary Outcome Measures

    1. Post operative depression [6 weeks]

      A disorder of mood characterized by sadness and loss of interest in usually satisfying activities, a negative view of the self and hopelessness, passivity, indecisiveness, suicidal ideations, loss of appetite, weight loss, sleep disturbances, and other physical symptoms. Some or all of these symptoms may be present, and depression can be categorized as mild, moderate, or severe/major according to scores measured on the Beck Depression Inventory II (BDI-II) (Diagnostic and Statistical Manual of Mental Health Disorders - Fourth Edition) (DSM-IV criteria).

    2. Post operative depression [12 weeks]

      A disorder of mood characterized by sadness and loss of interest in usually satisfying activities, a negative view of the self and hopelessness, passivity, indecisiveness, suicidal ideations, loss of appetite, weight loss, sleep disturbances, and other physical symptoms. Some or all of these symptoms may be present, and depression can be categorized as mild, moderate, or severe/major according to scores measured on the Beck Depression Inventory II (BDI-II) (Diagnostic and Statistical Manual of Mental Health Disorders - Fourth Edition) (DSM-IV criteria).

    Secondary Outcome Measures

    1. Perceptions of recovery [6 and 12 weeks]

      Includes biophysical recovery, return to activity, and return to social roles; perceptions focused on the absence or resolution of physiological and/or psychosocial clinical symptoms. (Perceptions of recovery were measured by the Postoperative Self-Report of Recovery Questionnaire (PSRRQ) over 12-weeks post-discharge.

    2. Perceptions of social support [6 and 12 weeks]

      Resources provided by others that can take the form of emotional support, instrumental aid, information, and positive feedback as to one's importance, capabilities or self worth. Social support was measured using the Shortened Social Support Scale (SSSS).

    3. Health services utilization [6 and 12 weeks]

      The consumption of health services (emergency room visits, regularly scheduled and unscheduled family physician visits and readmission to hospital) to meet health care needs as defined by the patient or the health care professional. This was measured by the number of health care visits/readmissions to hospital over 12-weeks post-discharge using the Postoperative Self Report of Recovery (PSRRQ).

    Other Outcome Measures

    1. Perceptions of peer support [12 weeks]

      Evaluation of the different aspects of peer support received (supportive interactions, relationship qualities, perceived benefits, satisfactions with support received) as measured by the Peer Support Evaluation Inventory (PSEI).

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    36 Years to 87 Years
    Sexes Eligible for Study:
    Male
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • English speaking

    • 35 years of age

    • undergoing first-time traditional (sternotomy approach) CABG surgery

    • an uncomplicated postoperative course

    • standard length of hospital stay (four to eight days)

    • had a telephone in the home

    • able to hear telephone conversation.

    Exclusion Criteria:
    • had cardiac surgery procedures other than CABG surgery

    • resided in a nursing home or long term care facility

    • had any neurological or psychiatric disorder that may have impeded ability to self reflect or communicate

    • had emergent cardiac surgery

    • had sustained in-hospital post surgical complications of major significance (i.e., stroke, GI bleed, cardiac tamponade, renal failure, cardiac arrest, major sepsis of any origin, deep sternal wound infection, myocardial infarction with significant hemodynamic compromise)

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Southlake Regional Health Centre Newmarket Ontario Canada N2C6J5
    2 Sudbury Regional Hospital Sudbury Ontario Canada P3E2C6
    3 Sunnybrook Health Sciences Centre Toronto Ontario Canada M4G 1R7

    Sponsors and Collaborators

    • University of Calgary
    • Heart and Stroke Foundation of Canada
    • Canadian Council of Cardiovascular Nurses

    Investigators

    • Principal Investigator: Kathryn King, PhD, University of Calgary

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Tracey JF Colella, RN, PhD, University of Calgary
    ClinicalTrials.gov Identifier:
    NCT01775228
    Other Study ID Numbers:
    • 17897
    • UofC 17897
    First Posted:
    Jan 24, 2013
    Last Update Posted:
    Jan 24, 2013
    Last Verified:
    Jan 1, 2013
    Keywords provided by Tracey JF Colella, RN, PhD, University of Calgary
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jan 24, 2013