Clinical trial Recruiting at 1 site Interventional Ages 9 Months to 15 Months

Investigating the Role of Naps in Infant Memory Development

Official title: The Function of Biphasic Sleep in Infants

Run by University of Massachusetts, Amherst · NCT06399939 · Data updated 2026-11-12

This study is testing how taking naps affects memory development in babies aged 9 to 15 months.

Quick facts

Study typeInterventional
Ages9 Months to 15 Months
SexAll
Enrollment100 (estimated)
SponsorUniversity of Massachusetts, Amherst
Academic / other
Locations1 site (Amherst, Massachusetts)
StatusRecruiting
StartedSeptember 1, 2023
Main results expectedJanuary 31, 2028
Study endsJanuary 31, 2029
Registry record updatedNovember 4, 2026
Trial IDNCT06399939 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are infants who are 9 months old at enrollment and meet specific health criteria.

Probably not a fit

Patients who are premature, have developmental delays, or significant motor disabilities may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study examines how naps affect memory development in infants aged 9 to 15 months. Researchers will assess sleep patterns using a motion-detecting watch and brain activity electrodes while measuring memory through a deferred imitation task. Infants will be observed in both nap and wake conditions to determine the impact of sleep on memory recall. The study involves multiple visits over several months to track developmental changes in sleep and memory.

Why it matters

Potential benefit: If successful, this study could enhance understanding of sleep's role in cognitive development, potentially leading to improved sleep recommendations for infants.

How similar studies have gone: While the specific approach may be novel, previous studies have indicated that sleep plays a crucial role in memory development, suggesting potential for success.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. 9 months at the time of enrollment
2. normal birthweight (5.5 to 10 lbs) and gestational length (36-41 weeks)
3. must be willing and able to return for testing in 3 and 6 months (e.g., no plans to move out of the area)

Exclusion Criteria:

1. born premature (\<36 weeks gestational age)
2. receiving services due to developmental delays
3. visual or motor disability
4. score \<85 on cognitive and language composite scales and/or \<80 on the average of the two composites of the Bayley Scales of Infant Development Fourth Edition (BSID-IV) administered at the first session.
5. Infants' motor development (gross and fine motor) will also be assessed using the BSID-IV, and an adjusted cutoff of 73 will be used to exclude infants with significant motor delays (given the motoric nature of the task).
6. traveling beyond 1 time zone within 2 weeks prior to testing (phone screening)
7. fever or symptoms of respiratory illness at the time of testing (phone screening)
8. physical handicap that interferes with assessments (vision, hearing impairment; phone screening)
9. history of neurological injury such as history of seizures, brain tumor, or stroke (phone screening) Parents/guardians of potential participants will be contacted via phone and/or email, at which time the details of the study will be specified and inclusion/exclusion criteria will be reviewed.

Where it's running

  • University of Massachusetts, Amherst
    Amherst, Massachusetts, United States
    Recruiting

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.