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RecruitingNCT06277869Updated Mar 7, 2024

Effectiveness Trial of Thermal Jacket

A Phase 2 interventional study of Thermal Jacket and Kangaroo Mother Care in Preterm Neonate and Low Birthweight Neonate, sponsored by International Centre for Diarrhoeal Disease Research, Bangladesh. Recruiting at 3 sites in Bangladesh. Per ClinicalTrials.gov, last updated 2024-03-07.

Sponsored by International Centre for Diarrhoeal Disease Research, Bangladesh · Phase 2, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Dec 2024, 1 year 9 months ago, but the record still lists the study as recruiting.
  • Started Mar 2024; still recruiting 2 years 7 months later.
Phase
Phase 2
Study type
Interventional
Enrollment
300
Allocation
Non-randomized
Sex
All
01

Study summary

Globally, over 15 million neonates are born preterm each year. They account for approximately 30% of global neonatal deaths and 19% of total neonatal deaths in Bangladesh. They usually die because they cannot maintain normal temperature due to their weight, immature skin and underdeveloped thermal regulatory capacity of the brain.

Maintaining continuous Kangaroo Mother Care (KMC) for at least 16-20 hours/day, is sometimes not feasible for mothers or caregivers. In addition, we also have the challenge of keeping preterm or low birthweight (LBW) neonates warm during transportation.

The scientists at icddr,b, Johns Hopkins University, and George Mason University developed the thermal jacket for keeping preterm or LBW neonate warm. We have already completed the laboratory trial on mannquins and clinical safety trial among preterm or LBW neonates. Now, we propose to build on our previous work by systematically testing the effectiveness trial of the 'thermal jacket' among preterm or LBW neonates at clinical settings.

Hypothesis: Thermal jacket can increase the rate of euthermia among the preterm or LBW neonates in the selected health facilities in Bangladesh.

Objectives: The aim of this study is to test whether the thermal jacket can attain and maintain euthermia of preterm or LBW neonates in clinical settings of Bangladesh.

Read the detailed description

We will equip a cluster-randomized stepped-wedge trial design. We will select and onboard hospitals randomly from three districts in pre-intervention period which eventually go into post-intervention period. The study will be conducted in three phases. The pre-intervention period for eight weeks for baseline data collection. Then intervention period (introduce thermal jackets) for another 24 weeks, and post-intervention period for endline data collection for eight weeks. In the control phase, all the eligible neonates enrolled in the hospitals whose parents agree to participate in the study will be observed and monitored for their thermal status (euthermia, hypothermia, and hyperthermia). Once the hospitals shift to case phase the eligible neonates will be given with thermal jacket. The icddr,b team will observe and monitor the enrolled neonates' thermal status throughout the event period. For this study, the definition of an event is the data from an individual enrolled infant on six hours' basis. Thus, every twenty-four hours, we can collect four events from a single neonate. During thermal care uptake, let it be with KMC or thermal jacket, the axillary temperature of the enrolled neonates will be recorded every 60 minutes. Feeding history will be recorded until discharge. According to the national newborn health SOP, during both control and case phases, mothers will be encouraged to provide KMC. The thermal jacket will be offered to mother when KMC will be ceased or not given by the neonate's family members. The thermal jacket intervention will be ceased for each neonate if mother wants to provide KMC or doesn't wish to put the neonate on the thermal jacket anymore. Thermal jacket will be provided for the time period as long as mother or legal guardian wishes to keep their neonate in the jacket without any time limitation. Mothers or caregivers of each neonate will be provided with training on KMC and thermal jacket and due support during the uptake of the KMC and thermal jacket will be provided as well. The data those will be collected during the pre-phase will be the control data and data that will be collected during the post-phase will be the intervention data.

02

Conditions studied

  • Preterm Neonate
  • Low Birthweight Neonate

Keywords

  • Preterm neonate
  • Low birthweight neonate
  • Kangaroo Mother Care
  • Thermal Jacket
03

In context

Premature Birth

2,554 studies on the registry are indexed under Premature Birth; 498 are open to participants now.

This study's planned enrollment of 300 is above the median of 84 across 1,689 interventional studies indexed under Premature Birth.

Browse Premature Birth studies →

Lead sponsor

International Centre for Diarrhoeal Disease Research, Bangladesh is the lead sponsor of 197 studies on the registry; 28 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. KMC eligible neonates
  2. Heart rate 100-160 per minute
  3. Capillary Refill Time ≤ 3 sec
  4. Respiratory rate 30-59 per minute
  5. Breaths comfortable
  6. Pink in room air

Exclusion criteria

Exclusion Criteria:

  1. In nasogastric tube
  2. In oxygen therapy
  3. In intravenous fluid
  4. Sign of respiratory distress
  5. Prolonged or frequent apnea
  6. Major surgical problem
  7. Gross congenital anomaly
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Factorial assignment
Masking
None (open label)
Enrollment
300 participants (estimated)

Study arms

  • Experimental
    Thermal Jacket

    As a intervention, the enrolled preterm or low birthweight neonates gets the thermal jacket as well as Kangaroo Mother Care for thermal care.

    Device: Thermal Jacket · Procedure: Kangaroo Mother Care

  • Active comparator
    Kangaroo Mother Care

    As a control, the enrolled preterm or low birthweight neonates gets the conventional Kangaroo Mother Care only.

    Procedure: Kangaroo Mother Care

Interventions

  • DeviceThermal Jacket

    In the intervention group, the enrolled preterm or low birthweight eligible neonates gets the intervention Thermal Jacket as well as Kangaroo Mother Care.

  • ProcedureKangaroo Mother Care

    Skin-to-Skin care, provided by primary caregiver.

06

What researchers measure

Primary outcomes

  1. Body temperature of preterm or low birthweight neonates maintain the euthermic range.

    The primary outcome of this phase is attainment and maintenance of euthermia, defined as i. Having reached to 36.5⁰ C for hypothermic neonates at any point of a single event, ii. Maintaining euthermia throughout the event and iii. Having risen the temperature up to the euthermic range within 1 hour if at any point neonate goes below euthermic range. The endpoint of each event will be ascertained for every neonate during the pre-phase and intervention-phase in the same manner regardless of whether the thermal jacket is used.

    Time frame: 6 hours per event

07

Study locations

2 of 3 sites recruiting
  • Lakshmipur District Hospital
    Lakshmipur, Chattogram 3700, Bangladesh
    Recruiting
  • Kushtia 250 Bedded General Hospital
    Kushtia, Khulna 7000, Bangladesh
    Recruiting
  • Jamalpur 250 Beded General Hospital
    Jamalpur, Mymensingh 2000, Bangladesh
    Not yet recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 7, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06277869
Lead sponsor
International Centre for Diarrhoeal Disease Research, Bangladesh
Collaborators
Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh, Directorate General of Health Services (DGHS), Bangladesh, Poeticgem International Ltd
Responsible party
Sponsor
First posted
Feb 26, 2024
Start date
Mar 1, 2024
Primary completion
Dec 22, 2024 (estimated)
Completion
Dec 31, 2024 (estimated)
Last update
Mar 7, 2024

Study contacts

Anisuddin Ahmed, MS
Contact
anisuddin@icddrb.org
+8801755571024
M.A Salam Khan, MS
Contact
salamk@icddrb.org
88029886498
Anisuddin Ahmed, MS
principal investigator · International Centre for Diarrhoeal Disease Research, Bangladesh

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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