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
About this trial
This is an interventional treatment trial for Congenital Heart Disease focused on measuring congenital heart disease, massage, pediatric pain
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
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
NCT ID
NCT04416230
First Posted
May 22, 2020
Last Updated
June 1, 2020
Sponsor
Ohio State University
Collaborators
Nationwide Children's Hospital
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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