SmarToyGym
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- STATUS
- Recruiting
Summary
This project develops a SmarToyGym where sensorized, wireless toys are placed within the reach of infants to elicit body, arm/hand and leg movements. The objective is to conduct pilot testing of the SmartToyGm with atypical and typical infants. A battery of metrics will be identified to discriminate between high and low risk infants, thus allowing for earlier neurodevelopmental intervention.
Description
The Center for Rehabilitation at CHOP, along with the Department of Physical Medicine and Rehabilitation at the University of Pennsylvania School of Medicine and the Department of Bioengineering, is conducting a study with typically and atypically developing infants. We are developing a SmarToyGym where the toys are equipped with tiny internal sensors to measure how babies reach and play with them. The information we learn will help develop early treatments for infants at-risk for delays. Infants aged 3 to 11 months are eligible to participate, including those with and without developmental delays. What will participants be asked to do? • The study can be done at CHOP or at The Penn Institute for Rehab Medicine (18th & Lombard) • A physical therapist will administer a developmental evaluation • Participants will be asked to use the SmarToyGym for up to 5 consecutive days • SmarToyGym sessions will last approximately 15 minutes There is no direct benefit to you from taking part in this study. The knowledge gained from the study will be used to develop treatments for infants at-risk for developmental delay. You will be paid for your time.
Details
| Condition | Cerebral palsy, Developmental Disabilities, Growth & Development |
|---|---|
| Age | 1years - 1years |
| Clinical Study Identifier | TX4764 |
| Last Modified on | 19 February 2024 |
Eligibility
How to participate?
Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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