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The Effect of Thermal Heat Application on Colic in Infants

The Effect of Thermal Heat Application on Colic in Infants

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07435948
Enrollment
75
Registered
2026-02-27
Start date
2025-04-15
Completion date
2025-12-15
Last updated
2026-02-27

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

Conditions

Infantile Colics

Keywords

Infantile colic, Cherry pit pillow, Warm towel, Non-pharmacological treatment

Brief summary

This study is a randomized controlled experimental trial designed to evaluate the effectiveness of thermal heat applications-specifically cherry pit pillows and warm towels-on reducing colic symptoms in infants aged 0-3 months. The study compares infants receiving these non-pharmacological thermal interventions with a control group receiving routine care, measuring outcomes such as colic severity, crying duration, feeding, and sleep patterns.

Detailed description

Infantile colic is a common condition characterized by recurrent and prolonged crying episodes in healthy infants. Owing to the limited effectiveness of pharmacological treatments, there is a strong need for reliable non-pharmacological methods. This pre-test, post-test randomized controlled experimental study was conducted to investigate the effects of thermal heat application on colic in infants aged 0-3 months. The sample consists of 75 infants diagnosed with colic, who were randomly assigned into three equal groups using block randomization: a cherry pit pillow application group (n=25), a warm towel application group (n=25), and a control group (n=25). For the intervention groups, the heated materials (cherry pit pillow or warm towel) were applied to the infant's abdominal area for 15 minutes per session, three days a week, over a two-week period. The control group received routine care without any specific thermal intervention. Data to evaluate the effectiveness of the applications were systematically collected using the Family Introduction Form, the Infantile Colic Scale (ICS), and the 24-hour Colic Baby Diary.

Interventions

OTHERCherry Pit Pillow Application

Application of a heated cherry pit pillow to the infant's abdominal area to reduce colic symptoms.

OTHERWarm Towel Application

Application of a heated warm towel to the infant's abdominal area to reduce colic symptoms.

Sponsors

Istanbul University - Cerrahpasa
Lead SponsorOTHER
Uskudar University
CollaboratorOTHER
Istanbul Training and Research Hospital
CollaboratorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
0 Weeks to 12 Weeks
Healthy volunteers
No

Inclusion criteria

Infants diagnosed with infantile colic. Aged 0-12 weeks. Born at term (37-42 weeks gestational age). Birth weight between 2500-4500 grams.

Exclusion criteria

Premature birth (less than 37 weeks). Presence of any chronic disease or gastrointestinal anomaly. Lactose intolerance or cow's milk protein allergy. Infants who had taken medication in the previous 24 hours.

Design outcomes

Primary

MeasureTime frameDescription
Change in Daily Crying and Sleep DurationsDaily for 2 weeksThe daily durations of the infants' crying, sleeping, feeding, and normal behaviors were recorded using the 24-hour Colic Baby Diary (Barr Diary). This allows for objective analysis of the effectiveness of the thermal methods on crying frequency and sleep regularity.
Change in Infant Colic Scale (ICS) ScoresFrom baseline (pre-test) to 2 weeks (post-test)The scale assesses the severity of colic. It consists of 19 items and five sub-dimensions: cow's milk/soy protein allergy/intolerance, immature digestive system, immature central nervous system, difficult baby, and problematic parent-baby interaction. Items are rated on a Likert scale ranging from 1 to 6. A lower total score indicates a decrease in colic severity.

Countries

Turkey (Türkiye)

Contacts

PRINCIPAL_INVESTIGATORŞEYMA ŞANLI

Üsküdar UniversityÜsküdar University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 28, 2026