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Flexible Electronics for Early Assessment

Young Hands at Work and Play: Flexible Electronics for Early Assessment of Force Modulation and Planning in Children Born Prematurely

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03034785
Enrollment
33
Registered
2017-01-27
Start date
2017-08-02
Completion date
2021-05-04
Last updated
2022-05-03

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

Conditions

Very Low Birth Weight Infant

Brief summary

The morbidities associated with very low birth weight (VLBW) infants constitute a major health problem and a significant emotional and financial burden for families and our nation. The key to reducing this burden is early diagnosis. This research will be the first step towards intervention for cerebral growth and long-term neurodevelopmental morbidities of VLBW infants. The proposed research is to design and fabricate a new technological innovation in wearable soft-sensors, called flexi-mitts, for measuring force modulation and joint angles of the hand (wrist and fingers) of toddlers. Building upon the investigators' ongoing work, they plan to engineer stretchable electronics for safe, toddler-scaled flexi-mitts to measure planning and force modulation. The investigators' new flexi-mitt technology has the potential to provide a new diagnostic technology and the development of clinical assessment norms. With additional trials of the technology in large numbers of young children, it may be possible for clinicians and day care providers to eventually make measurements of planning and force modulation in play settings.

Interventions

DEVICEFlexiMitt

The proposed research designs and fabricates a new technological innovation in wearable soft-sensors, called flexi-mitts, for measuring force modulation and joint angles of the hand (wrist and fingers) of toddlers.

Sponsors

Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
CollaboratorNIH
Beth Israel Deaconess Medical Center
CollaboratorOTHER
Wyss Institute at Harvard University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DEVICE_FEASIBILITY
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
13 Months to 60 Months
Healthy volunteers
Yes

Inclusion criteria

Children Born Prematurely (Preterm) - Pilot Studies: * Ages 13-60 months (with the target ages around 18, 24, and 30 months) * Very low birth weight (less than 1500 grams) * Born between 28 and 33 weeks * Parent/Legal guardian provides written consent * Parent/Legal guardian is willing to facilitate testing with child (and may be included in photos/videos as a result) * Otherwise healthy condition Longitudinal Study: * Ages 13-60 months (with the target age around 24 months) at the time of enrollment * Very low birth weight (less than 1500 grams) * Born between 28 and 33 weeks * Parent/Legal guardian provides written consent * Parent/Legal guardian is willing to facilitate testing with child (and may be included in photos/videos as a result) * Otherwise healthy condition Typically Developing Children (Term) - Pilot Studies: * Ages 13-60 months (with the target ages around 18, 24, and 30 months) * Born at full term (37 weeks or later) * Healthy, with no history of neurological problems or musculoskeletal disorders, self-reported by parent or legal guardian * Parent/Legal guardian provides written consent * Parent/Legal guardian is willing to facilitate testing with child (and may be included in photos/videos as a result) Longitudinal Study: * Ages 13-60 months (with the target age around 24 months) at time of enrollment * Born at full term (37 weeks or later) * Healthy, with no history of neurological problems or musculoskeletal disorders, self-reported by parent or legal guardian * Parent/Legal guardian provides written consent * Parent/Legal guardian is willing to facilitate testing with child (and may be included in photos/videos as a result)

Exclusion criteria

Both Preterm and Term * Child has a history of/or currently exhibits any severe neurological complications, such as perinatal intraventricular hemorrhage (Grade 3 or 4) or periventricular leukomalacia * The participant is a child of a PI or other IRB-approved study team member * Parent/legal guardian does not provide consent or is unwilling to facilitate testing with child

Design outcomes

Primary

MeasureTime frameDescription
Design and Fabricate FlexiMittsAnticipated Year 1To measure joint angles and force
Demonstrate SafetyAnticipated Year 1Bench tests of material failure (i.e., stretch deformity and compositional integrity)
Examine group differences between Groups 1 and 2Anticipated Year 2 through 4To examine group differences in force modulation and joint angles
Examine longitudinal differences between Groups 1 and 2Anticipated Year 2 through 4To examine longitudinal changes in force modulation and joint angles at 24 and 30 months

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026