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NCT Number: NCT03840083

Sleep-dependent Learning in Aging

The specific objective of this proposed research is to understand whether deficits in sleep-dependent memory changes reflect age-related changes in sleep, memory, or both. The central hypothesis is that changes in both memory and sleep contribute to age-related changes in sleep-dependent memory processing. To this end, the investigators will investigate changes in learning following intervals of sleep (overnight and nap) and wake in young and older adults.

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Key information

Conditions

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Massachusetts

Amherst, Massachusetts, 01003, United States

Location status: Recruiting

Location contact

Mary Emma Searles

CONTACT

[email protected]

413-545-4831

About this study

Exp 1: Using neuroimaging, the investigators will consider whether differences in brain areas engaged during memory encoding contribute to age-related changes in sleep-dependent memory consolidation for a word-pair learning task.

Exp 2: The investigators will examine the rate of memory decay between encoding and sleep using two probes of declarative memory (word-pair learning and visuo-spatial learning).

Exp 3: The investigators will provide additional opportunity for encoding of the word-pair and visuo-spatial learning tasks.

Exp 4: Using neuroimaging, the investigators will examine neural engagement during encoding and performance following intervals of sleep and wake.

Exp 5: The investigators will examine the rate of decay of motor sequence learning.

Exp 6: The investigators will examine whether enhanced training ('overtraining') improves sleep-dependent memory consolidation for older adults.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 18-80 yrs
  • Healthy sleeper
  • No diagnosed sleep or neurodegenerative disorder

Exclusion criteria

  • Past diagnosis of any sleep disorder or evidence of a sleep disorder as assessed by self-reported sleep quality assessments, a standardized diagnostic interview, and an acclimation night of polysomnography. Using acclimation-night polysomnography, participants will be excluded with an Apnea-Hypopnea Index >15; a Period-Limb Movement in Sleep index of >15/hr; sleep-onset latency > 45 min (indicative of insomnia); or sleep efficiency < 80% (see Edinger et al., Sleep, 2004). In cases in which questions arise regarding a participants' inclusion or sleep records, a practicing neurologist board-certified in sleep medicine will review the documentation.
  • Past diagnosis neurological illness or head injury
  • Reported average sleep per night < 5 or > 9 hrs
  • Current employment involving shift work or an inability to keep a regular sleep schedule during the week prior to testing
  • Current use of psychotropic, recreational drugs, or sleep-altering medications (sleep medications, cold medicines within the past week, clonidine, sympathomimetic stimulants)
  • Daily caffeine intake of > 4 cups (coffee, tea, colas)
  • Weekly alcohol intake of > 10 cups
  • Pregnancy or < 12 months post-partum
  • History of bipolar disorder, mania, or current evidence of depression as measured by Beck Depression Inventory score > 25
  • Abnormal sleep (e.g., shift work, travel across >2 time zones within the past 3 months).
  • Diagnosis of any Axis I disorder, neurological illness or head injury (according to Demographic and Health History form);
  • Score indicative of cognitive dysfunction (subtest scores < 40)
  • Beck Depression Scale score indicative of depression (> 19).

Additionally, individuals will be excluded from magnetic resonance imaging studies (Exps 1, 4) for:

  • Left handed or ambidextrous
  • Claustrophobia
  • Presence of metal (thoroughly screened via questionnaire and metal detector)
  • Pregnancy

Treatment and study plan

sleep

Behavioral

Participants will sleep (either a mid-day nap or normal overnight sleep)

Primary outcomes

  1. Change in memory accuracy for intervention compared to control

    Time frame: 2 hours (Experiments 1,4) or 12 hours (Experiments 2,3,5,6)

    We will measure memory accuracy before the sleep/wake interval and subtract this from memory accuracy after the sleep wake interval. If sleep benefits memory then this value will be greater in the sleep condition compared to the wake condition.

Sponsors and collaborators

Lead sponsor

University of Massachusetts, Amherst

Other

Registry information

Official study title

What is Sleep's Role in Alzheimer's Disease? Insight From Healthy Aging

Important dates

Study start
2018
Primary completion
2025
Study completion
2025
First posted
Feb 15, 2019
Registry last updated
Apr 3, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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