- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04285437
The Effects of Massage Therapy on Term Neonates Development and on Maternal Bonding
The Effects of Massage Therapy on Mental and Physical Development of Term Neonates and on Maternal Bonding.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Infant Massage has been known for a long time, almost as far back as the first time it was recorded around 1800 BC. This was one of the original forms of medicine before the medical revolution broke out in the 1940s.
To date, more than 600 studies have been published on the effects of weight gain on massaged infants, primarily in preterm infants. In addition, the latest research also helps identify other effects such as shortening hospital time, better sleep, reducing pain, crying less, strengthen immunity, reducing bilirubin in neonates with jaundice.
On the other hand, the effect of the "parent direct massage for children" is also determined, the reports show an improvement in the parent-child interaction, increase breastfeeding, and reduce breastfeeding. The rate of postpartum depression reduced significantly.
Steps to proceed
- Step 1: Randomly select 2 groups of mother- term neonate pairs by letting every mother, who matching with eligibility criteria, draw 1 of 120 same color and size lotteries in which include 1 to 120 numbers randomly drawn from a web page https://stattrek.com/statistics/random-number-generator.aspx .
There are 2 groups of mother - term neonate pairs (60 pairs each):
- Group M: neonates are massaged by their mothers during the first 2 months after birth. Mothers in this group will be given instructions on breastfeeding, and massage therapy (by principal investigator as International Association of Infant Massage Certified Instructor) in 2 days before discharge, and mothers will record "Parenting Dairy" form (The diary includes the number of defecation times, the number of spitting up times, the number of crying times over 15 minutes, the number of massage times, and the sleep time during the day)
Group X: neonates are not massaged. Mothers in this group will be given instructions on breastfeeding only, and they will record "Dairy of taking care baby" form like the other group.
- Step 2: At 1 day after discharge, the investigator make a phone call with mothers of group M to track and remind them massage for their babies.
- Step 3: At the time of 10 days before the baby turn 1 month - old and 2 month - old, the investigator make a phone call with mothers in both groups to track and remind massage for children (group M), as well as the record "Parenting Dairy" (both groups)
- Step 4: At the time the child turn 1 month - old and 2 month - old, the investigator make a home visit to both groups, let mothers perform Edinburgh Postnatal Depression Scale, collect data from "Parenting Dairy", assess the height - weight - head circle of the babies.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Ho Chi Minh City, Vietnam, 70000
- Recruiting
- University of Medicine and Pharmacy
-
Contact:
- Linh Dao Nguyen Phuong, MD
- Phone Number: +84902893839
- Email: bs.dnplinh@gmail.com
-
Contact:
- Duong Pham Diep Thuy, Ph.D, MD
- Phone Number: +84908143227
- Email: thuyduongpd@gmail.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria: Group of mother and neonate at Neonatal Department of Children Hospital II, Ho Chi Minh City
- neonate: full term, not low birth weight, 0 - 15 days of age, diagnosed with one of the following conditions and has been treated stably: uncomplicated neonatal infection, uncomplicated pneumonia, non umbilical cord infection, uncomplicated neonatal jaundice
- mother: live in Ho Chi Minh City
Exclusion Criteria: If the mother or neonate has the criteria to eliminate:
- Mother with mental illness, developmental disorder, prenatal depression, not directly caring for children.
- Neonate with multiple deformities, asphyxia, severe jaundice with complication, cow's milk allergy, heart/ lung/central nervous system defects.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: massage
neonates are massaged by their mother during the first 2 months after birth.
|
Mother will be trained how to massage their babies by International Association of Infant Massage (IAIM) Certified Infant Massage Instructor, and then their babies will be massaged by themselves during the first 2 months after birth.
|
|
No Intervention: control
neonates are not massaged.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The rate of pairs that have Edinburgh Postnatal Depression Scale scored > 12
Time Frame: at the day baby turns 1 month of age
|
When home visiting, the investigator let the mother do Edinburgh Postnatal Depression Scale
|
at the day baby turns 1 month of age
|
|
The rate of pairs that have Edinburgh Postnatal Depression Scale scored > 12
Time Frame: at the day baby turns 2 month of age
|
When home visiting, the investigator let the mother do Edinburgh Postnatal Depression Scale
|
at the day baby turns 2 month of age
|
|
Change of the number of crying times over 15 minutes at 2 month - old - infant
Time Frame: 2 months after birth
|
When home visiting, the investigator collect from "Parenting Dairy"
|
2 months after birth
|
|
The rate of pairs that have breastfeeding
Time Frame: at the day baby turns 1 month of age
|
When home visiting, the investigator collect from "Parenting Dairy"
|
at the day baby turns 1 month of age
|
|
The rate of pairs that have breastfeeding
Time Frame: at the day baby turns 2 month of age
|
When home visiting, the investigator collect from "Parenting Dairy"
|
at the day baby turns 2 month of age
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The mean of Edinburgh Postnatal Depression Scale
Time Frame: at the day baby turns 1 month of age
|
When home visiting, the investigator let the mother do Edinburgh Postnatal Depression Scale
|
at the day baby turns 1 month of age
|
|
The mean of Edinburgh Postnatal Depression Scale
Time Frame: at the day baby turns 2 month of age
|
When home visiting, the investigator let the mother do Edinburgh Postnatal Depression Scale
|
at the day baby turns 2 month of age
|
|
Change of the number of defecation times at 2 month - old - infant
Time Frame: 2 months after birth
|
When home visiting, the investigator collect from "Parenting Dairy"
|
2 months after birth
|
|
Change of the number of spitting up at 2 month - old - infant
Time Frame: 2 months after birth
|
When home visiting, the investigator collect from "Parenting Dairy"
|
2 months after birth
|
|
Change of weight at 2 month - old - infant
Time Frame: 2 months after birth
|
When home visiting, the investigator assess the weight of infant
|
2 months after birth
|
|
Change of height at 2 month - old - infant
Time Frame: 2 months after birth
|
When home visiting, the investigator assess the height of infant
|
2 months after birth
|
|
Change of head circle at 2 month - old - infant
Time Frame: 2 months after birth
|
When home visiting, the investigator assess the head circle of infant
|
2 months after birth
|
Collaborators and Investigators
Investigators
- Study Chair: Tuan Le Minh, Ph.D, MD, Research Department, UMP
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 414A/ĐHYD-HĐĐĐ
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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