Skip to content

The effect of a maternal, educational, supportive and care program on treatment of infantile colic pain

The effect of a maternal, educational, supportive and care program on sleeping, pain and crying rate due to colic in 1-5 months infants

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20171102037187N2
Enrollment
88
Registered
2018-02-23
Start date
2018-01-29
Completion date
Unknown
Last updated
2018-03-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

infants colic. R10.4 Other and unspecified abdominal pain. Abdominal tenderness NOS Colic: NOS infantile

Interventions

Intervention 1: In the case of infants who suffer from colic and have their colic approved by the doctor and are among the criteria for entering the study, parents are informed by written consent. Int

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Days to 5 Months

Inclusion criteria

Inclusion criteria: Have exclusive breastfeeding. Between 1 and 5 months. The infant has no autoimmune congenital or nutritional problem. At birth, the term of birth is more than 2500 grams. Appropriate weighing of the infant at that age is based on the percentile in the normal range. No skin lesions in breastfeeding and maternity.

Exclusion criteria

Exclusion criteria: Good poor feeding. Use of chemical drugs such as anti-pneumonia and ... at the time of the intervention. The child has a history of surgery and swelling. Exclusion of exclusive breastfeeding. The child now has an acute illness, such as a cold, etc.

Design outcomes

Primary

MeasureTime frame
Pain colic in infants. Timepoint: The severity of colic symptoms in infants before and after intervention in each group is calculated on the third and seventh day of treatment, and each group will be compared on the third and the third day of treatment separately from before intervention (due to taking the third day of treatment, the mean of the treatment for the infant and the day Seventh is the end of intervention treatment). Method of measurement: In both groups, mothers will complete the checklist based on the criteria for pain relief for severity of crying and hours for infant.The questionnaire includes a tool for evaluating colic pain, Visual Analogue Scale.

Secondary

MeasureTime frame
The amount of colic pain, infant crying, the frequency of crying, the duration of infancy and the severity of infant crying. Timepoint: Weekly (as the basal stage) record the infant's cry and sleep at night. In the second stage (as an intervention stage), mothers will be advised to run an educational-support-care program for a period of 8 days. Method of measurement: A researcher-made instrument that has four parts: maternal and infant characteristics, and breastfeeding pattern, maternal nutritional instrument, incubation colic assay (the main tool for the dependent variables), Visual Analogue Scale, including the duration of crying and its frequency in 24 Hours is.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactTahereh Sadeghi

Mashhad University of Medical Sciences

SadeghiT@mums.ac.ir+98 51 3859 1511

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026