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Benefits of Nicotinamide Riboside Upon Cognition and Sleep
Plain-language guide to NCT05500170: not phased randomized trial of NAD+, 50 participants. Who took part, design and what was measured.
Key Facts
- Registry ID
- NCT05500170
- Phase
- not phased
- Status
- recruiting participants
- Start
- 2023-04-04
- Completion (planned or actual)
- 2027-08-30
- Participants
- 50 (estimated)
- Design
- randomized, single-blind, supportive_care
- Conditions studied
- Cognitive Impairment; Sleep Quality
- Results posted
- not yet
What This Study Did, in Plain Language
What Was Tested
The trial (not phased) is built around NAD+.
It had two arms (groups): Intervention (experimental) and Placebo (placebo comparator).
The registry classes the interventions as dietary supplement.
More on the Plan
Ten percent of adults aged ≥ 65 years and fifty percent of adults ≥ 85 years exhibit cognitive impairment.
Consequently, millions of Americans are at risk for both cognitive impairment, including Alzheimer's Disease and other dementias, and disrupted sleep.
Importantly, sleep disturbances and mild cognitive impairment may appear several years before the development of clinical dementia.
Who Took Part
The registry lists 50 planned participants were the target.
It was open to people of any sex aged from 65 years up to 85 years.
Healthy volunteers could join, not only people with the condition.
Examples of who could join: Sleep Quality. Pittsburgh Sleep Quality Index (PSQI) global score \>5.
The full record lists 1 inclusion and 1 exclusion criteria.
How the Study Was Run
Design: randomized, parallel-group and single-blind.
The participants were allocated by chance, so the NAD+ group and the comparison group should start out alike.
Groups ran in parallel: each of the participants stayed in one arm throughout.
In this single-blind NAD+ study one party knew the assignments and the other did not.
Those kept unaware of assignments: participant.
It started in 2023-04-04 with completion listed for 2027-08-30.
It ran at 3 sites in United States (3).
Its stated primary purpose is supportive care.
What Was Measured
Researchers chose this as the main measure: Sleep Quality Assessment (time frame: Change from baseline to endpoint at 12 weeks).
It also tracked 1 secondary outcome, for example Cognitive function.
What This Means in Plain Language
Put simply, this is a not phased, randomized trial of NAD+ in 50 people.
It is still recruiting; no results are posted to the registry yet, so nothing here describes outcomes.
More context: the NAD+ compound page, all human trials.
Our Notes on the Compound
NAD+: The coenzyme that accepts electrons at complex I.
Related Pages
Source: ClinicalTrials.gov record. This explanation is written by PeptideWhiz from the public record. For research and education only. Not medical advice; no dosing information is given.