Evaluating the Effects of tDCS on Sleep and Cognition in Healthy Older Adults
NCT ID: NCT06938672
Last Updated: 2025-07-04
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
23 participants
INTERVENTIONAL
2025-07-31
2025-10-31
Brief Summary
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The main questions it aims to answer are:
* Can a short (20-minute) tDCS session before a nap improve sleep patterns during the nap?
* Since these sleep patterns are linked to memory and attention, can tDCS also improve thinking skills after the nap?
* Are two tDCS session more effective than one for improving nap sleep and thinking skills?
Participants will:
• Be required to come to the university for testing over four days.
During each session they will:
* Complete computer based-tasks to assess memory and thinking.
* Receive a 20-minute session of either real (active) or fake (placebo) tDCS.
* Take a short, monitored nap while researchers measure sleep activity (using polysomnography - a gold-standard, non-invasive sleep monitoring tool).
* Complete an easy-to-use sleep test at home on the nights after the naps.
* Wear a lightweight watch (called an Actiwatch) throughout the study period to track sleep and movement.
* Complete daily sleep diaries.
By taking part, participants will help researchers understand whether tDCS can improve sleep during naps and, in turn, support memory and thinking skills. This research could lead to better treatments for sleep problems, help protect brain health, and reduce the risk of dementia as people age. The brain stimulation in this study may also help improve their sleep and cognition.
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Detailed Description
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Transcranial direct current stimulation (tDCS), a non-invasive technique that modulates brain activity, shows promise for enhancing both sleep and cognition. However, existing studies have significant methodological limitations. Notably, very few have investigated 'offline' tDCS -where stimulation is applied before sleep- to assess objective sleep changes using polysomnography (PSG). Instead, most research has relied on subjective measures, consistently finding that offline tDCS enhances perceived sleep quality, especially with repeated stimulation sessions. Importantly, offline tDCS may be more feasible for use outside laboratory settings compared to 'online' approaches, where stimulation is applied during sleep, making it a more scalable intervention.
Furthermore, delivering tDCS before a daytime nap, rather than nocturnal sleep, offers additional advantages by reducing participant burden, particularly in older adults. Studies applying tDCS during a nap in older adults have shown improvements in objective sleep microstructure and declarative memory. By contrast, studies applying tDCS during nocturnal sleep have reported inconsistent results. Despite its potential benefits, no studies have explored the effects of an offline, nap-based tDCS approach on objective sleep outcomes.
Additionally, few studies have examined whether repeated sessions of offline tDCS might amplify its effects on objective PSG-measured sleep. While repeated sessions have been shown to positively influence subjective sleep outcomes, it remains unclear whether the same benefits apply to objective sleep metrics. This study will address this gap by investigating whether two sessions of offline tDCS, compared to one, are necessary to improve objective sleep outcomes.
In summary, this study aims to determine whether offline tDCS applied prior to a nap can enhance objective sleep during a daytime nap and improve post-nap cognitive performance in older adults. If effective, this low-burden, non-invasive intervention could serve as a practical tool for promoting healthy aging and reducing dementia risk.
The primary objectives of this randomised, placebo-controlled crossover trial are:
To evaluate the impact of offline tDCS on objective sleep microstructure and architecture during naps.
To assess the effects of tDCS on post-nap cognitive performance. To examine the cumulative effect of two tDCS sessions upon objective sleep and cognition, compared to one.
Conditions
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Study Design
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RANDOMIZED
CROSSOVER
PREVENTION
DOUBLE
Study Groups
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Active Transcranial Direct Current Stimulation (tDCS)
Transcranial direct current stimulation. Participants will experience a 20-minute session of active tDCS (1.2 mA) on two consecutive days.
Active Transcranial Direct Current Stimulation (tDCS)
Active transcranial direct current stimulation (tDCS). Participants will experience a 20-minute session of active tDCS (1.2 mA) on two consecutive days.
Placebo Transcranial Direct Current Stimulation (tDCS)
Transcranial direct current stimulation. Participants will experience a 20-minute session of placebo tDCS on two consecutive days.
Placebo Transcranial Direct Current Stimulation (tDCS)
Placebo Transcranial direct current stimulation (tDCS): Participants will experience a 20-minute session of placebo tDCS on two consecutive days.
Interventions
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Placebo Transcranial Direct Current Stimulation (tDCS)
Placebo Transcranial direct current stimulation (tDCS): Participants will experience a 20-minute session of placebo tDCS on two consecutive days.
Active Transcranial Direct Current Stimulation (tDCS)
Active transcranial direct current stimulation (tDCS). Participants will experience a 20-minute session of active tDCS (1.2 mA) on two consecutive days.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Speak fluent English
* Be cognitively healthy
* A self-reported good sleeper, with a regular sleep pattern
Exclusion Criteria
* Self-reported neurodegenerative dementia or other neurological disorders
* Self-reported relevant sleep disorders or disturbances
* Those with irregular sleep schedules (i.e. night shift workers)
* A PSQI score above 5 (as this is associated with significant sleep disturbance)
* Relevant skin allergies
* Taking medication that affects the central nervous system or sleep, or consume caffeine, alcohol or cigarettes excessively
* Metallic or electronic implants
60 Years
ALL
Yes
Sponsors
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Northumbria University
OTHER
Responsible Party
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Principal Investigators
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Rosie H Musgrave, BA Hons, RPSGT
Role: PRINCIPAL_INVESTIGATOR
Northumbria University
Locations
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Northumbria University
Newcastle upon Tyne, , United Kingdom
Countries
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Facility Contacts
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Other Identifiers
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2025-6636-10284
Identifier Type: -
Identifier Source: org_study_id
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