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Post-Op Massage in Infants With Congenital Heart Disease

Primary Purpose

Congenital Heart Disease

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
massage
quiet time
Sponsored by
Ohio State University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Congenital Heart Disease focused on measuring congenital heart disease, massage, pediatric pain

Eligibility Criteria

1 Day - 12 Months (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Infants born with complex congenital heart disease requiring surgical intervention
  • less than 12 months old
  • undergoing first surgical procedure

Exclusion Criteria:

  • on paralytics post-operatively
  • cardiorespiratory instability
  • on-going cardiac pacing

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Active Comparator

    Arm Label

    Massage

    Quiet Time

    Arm Description

    Infants randomized to the massage intervention received a 30 minute massage daily for the 7 day study.

    Infants randomized to the Quiet Time intervention experienced a 30 minute time during which non-essential clinical caregiving tasks were restricted.

    Outcomes

    Primary Outcome Measures

    Post-operative pain score
    FLACC score: behavioral observation of face, legs, activity, cry, consolability
    Change in post-operative pain score with intervention
    FLACC score: behavioral observation of face, legs, activity, cry, consolability
    Heart rate
    heart rate in beats per minute
    Respiratory rate
    respiratory rate in breaths per minute
    Oxygen saturation
    oxygen saturation percentage
    Change in heart rate with intervention
    heart rate in beats per minute
    Change in respiratory rate with intervention
    respiratory rate in beats per minute
    Change in oxygen saturation with intervention
    oxygen saturation percentage

    Secondary Outcome Measures

    Full Information

    First Posted
    May 22, 2020
    Last Updated
    June 1, 2020
    Sponsor
    Ohio State University
    Collaborators
    Nationwide Children's Hospital
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04416230
    Brief Title
    Post-Op Massage in Infants With Congenital Heart Disease
    Official Title
    The Effects of Massage on Pain After Pediatric Cardiothoracic Surgery
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    June 2020
    Overall Recruitment Status
    Completed
    Study Start Date
    May 1, 2012 (Actual)
    Primary Completion Date
    August 3, 2013 (Actual)
    Study Completion Date
    May 30, 2014 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Ohio State University
    Collaborators
    Nationwide Children's Hospital

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    The primary aims of the proposed study are to pilot test the effectiveness of daily massage on pain and clinical outcomes in infants who have undergone cardiothoracic surgery. The secondary aim is to explore relationships among massage, pain scores, and other variables potentially affecting pain scores, including parental anxiety, severity of cardiac defect, and severity of pain. Specific Aim 1: To compare effects of massage on infant pain and clinical outcomes between two groups over time: infants receiving post-operative massage seven days post-operatively and infants receiving a comparable time of restricted non-essential caregiving seven days post-operatively. Specific Aim 2: To compare pain scores and physiologic responses before and after intervention in two groups: infants receiving post-operative massage and infants receiving a comparable time of restricted non-essential caregiving. Specific Aim 3: To examine potential moderators of pain response in the massage intervention group before and after receiving massage.
    Detailed Description
    We used a two-group randomized clinical trial design with a sample of 60 infants with complex congenital heart disease (CCHD) between 1 day and 12 months of age following their first cardiothoracic surgery. Both groups received standard post-operative care. In addition, Group 1 received a daily 30-minute restricted non-essential direct caregiving time (Quiet Time), and Group 2 received a daily 30-minute massage. Interventions continued for seven consecutive days. Pain was measured 6 times daily using the Face, Legs, Activity, Cry, Consolability Pain Assessment Tool (FLACC). Average daily doses of analgesics were recorded. Heart rates (HR), respiratory rates (RR), and oxygen saturations (SpO2) were recorded continuously. Daily averages and pre- and post- intervention FLACC scores and physiologic responses were analyzed using descriptive statistics, generalized linear mixed models (GLMM) for repeated measures, latent growth models, and/or regression discontinuity analysis. Fentanyl-equivalent narcotic values were used as a time-varying covariate.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Congenital Heart Disease
    Keywords
    congenital heart disease, massage, pediatric pain

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Model Description
    The intervention consisted of a massage given by a licensed massage therapist on each of seven consecutive days beginning on the day of surgery (Day 1). The massage included 30 minutes of Swedish massage on the infant's accessible upper extremities, lower extremities, head, face, and back. Standard precautions were used, including proper hand hygiene and the use of gloves when needed for infection control. Infants randomized to the comparison group received a 30 minute quiet time (QT) period during which non-essential caregiving tasks were restricted. During QT, clinicians were asked to avoid direct clinical caregiving activities, i.e. activities requiring physical contact with the infant.
    Masking
    Care ProviderOutcomes Assessor
    Masking Description
    Research assistants scoring participant pain were blinded to group.
    Allocation
    Randomized
    Enrollment
    65 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Massage
    Arm Type
    Experimental
    Arm Description
    Infants randomized to the massage intervention received a 30 minute massage daily for the 7 day study.
    Arm Title
    Quiet Time
    Arm Type
    Active Comparator
    Arm Description
    Infants randomized to the Quiet Time intervention experienced a 30 minute time during which non-essential clinical caregiving tasks were restricted.
    Intervention Type
    Behavioral
    Intervention Name(s)
    massage
    Intervention Description
    The massage included 30 minutes of gentle friction, kneading, stroking, and passive touch on the infant's accessible upper extremities, lower extremities, head, face, and back.
    Intervention Type
    Behavioral
    Intervention Name(s)
    quiet time
    Intervention Description
    During quiet time, the infant received a 30 minute quiet time (QT) period during which non-essential caregiving tasks were restricted. During QT, clinicians were asked to avoid direct clinical caregiving activities, i.e. activities requiring physical contact with the infant.
    Primary Outcome Measure Information:
    Title
    Post-operative pain score
    Description
    FLACC score: behavioral observation of face, legs, activity, cry, consolability
    Time Frame
    Daily average for 7 days
    Title
    Change in post-operative pain score with intervention
    Description
    FLACC score: behavioral observation of face, legs, activity, cry, consolability
    Time Frame
    Daily for 7 days
    Title
    Heart rate
    Description
    heart rate in beats per minute
    Time Frame
    Daily average for 7 days
    Title
    Respiratory rate
    Description
    respiratory rate in breaths per minute
    Time Frame
    Daily average for 7 days
    Title
    Oxygen saturation
    Description
    oxygen saturation percentage
    Time Frame
    Daily average for 7 days
    Title
    Change in heart rate with intervention
    Description
    heart rate in beats per minute
    Time Frame
    Daily for 7 days
    Title
    Change in respiratory rate with intervention
    Description
    respiratory rate in beats per minute
    Time Frame
    Daily for 7 days
    Title
    Change in oxygen saturation with intervention
    Description
    oxygen saturation percentage
    Time Frame
    Daily for 7 days

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    1 Day
    Maximum Age & Unit of Time
    12 Months
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Infants born with complex congenital heart disease requiring surgical intervention less than 12 months old undergoing first surgical procedure Exclusion Criteria: on paralytics post-operatively cardiorespiratory instability on-going cardiac pacing
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Tondi M Harrison, PhD, RN
    Organizational Affiliation
    The Ohio State University and Nationwide Children's Hospital
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No
    IPD Sharing Plan Description
    There is not a plan to make individual participant data available.
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    Post-Op Massage in Infants With Congenital Heart Disease

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