Effect of ZenRest™ Lotus Seed & Rice Germ Extract Blend on Sleep Quality in Menopausal Women
25. juni 2026 opdateret af: Nutraland USA, Inc.
A Randomized, Double-Blind, Placebo-Controlled, 6-Week Pilot Study to Evaluate the Effect of ZenRest™ Lotus Seed & Rice Germ Extract Blend on Sleep Quality in Menopausal Women
The goal of this clinical trial is to learn if ZenRest™ (Lotus Seed & Rice Germ Extract Blend) can help improve sleep quality in menopausal women aged 40-65 with mild-to-moderate sleep complaints.
The main questions it aims to answer are:
- Does taking ZenRest™ daily improve subjective, participant-reported sleep quality compared to a placebo?
- Does ZenRest™ improve objective sleep metrics, specifically sleep efficiency, when monitored via an Oura Ring wearable device?
- Does the extract improve secondary sleep and lifestyle factors, such as insomnia severity, daytime sleepiness, and vitality? Researchers will compare ZenRest™ to a placebo (a look-alike capsule that contains no active ingredients) to see if the botanical blend has a measurable effect on sleep quality.
Studieoversigt
Status
Ikke rekrutterer endnu
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
ZenRest™ is a proprietary blend of Lotus Seed Extract (Nelumbo nucifera) and Rice Germ Extract (Oryza sativa).
This trial evaluates the physiological effects of continuous daily intake (50 mg/day) over a 6-week period, specifically targeting menopausal women with mild-to-moderate sleep complaints.
The study utilizes a fully decentralized clinical trial framework.
Behavior and physiological metrics are collected remotely utilizing home-based, integrated smart ring wearable tracking methodologies to minimize participant burden.
In addition to evaluating subjective sleep indices by measuring changes in the Pittsburgh Sleep Quality Index (PSQI) from baseline to end of study, the protocol investigates continuous objective sleep architecture by assessing daily wearable ring data.
This secondary analysis utilizes the Oura Ring platform to evaluate advanced parameters, including sleep efficiency, total sleep time, deep sleep and REM sleep duration, sleep latency, and resting heart rate and heart rate variability dynamics.
Undersøgelsestype
Interventionel
Tilmelding (Anslået)
60
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiekontakt
- Navn: Alethios, Inc.
- Telefonnummer: 650-206-8006
- E-mail: support@alethios.com
Undersøgelse Kontakt Backup
- Navn: Dr. Bill Clark, Ph.D.
- Telefonnummer: 727-365-3420
- E-mail: drbill@natprologix.com
Studiesteder
-
-
California
-
San Francisco, California, Forenede Stater, 94109
- Alethios, Inc.
-
Kontakt:
- Zeenia Framroze, BA MPhil
- Telefonnummer: 650-206-8006
- E-mail: support@alethios.com
-
-
Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Ja
Beskrivelse
Inclusion Criteria:
- Female, aged 40-65 years at time of enrollment
- Confirmed menopausal status: (a) natural menopause (≥12 consecutive months of amenorrhea without other clinical cause), or (b) surgical menopause (bilateral oophorectomy with documented date of procedure)
- Positive onboarding sleep screener: rates sleep quality as "Fairly Bad" or "Very Bad" AND reports sleep difficulty at least once per week in the prior month
- PSQI global score >5 at T0 baseline assessment (formal eligibility gate)
- Owns and actively uses an Oura Ring Generation 4 at time of enrollment
- Demonstrates ≥80% Oura Ring wear compliance in the 30 days prior to enrollment, confirmed via Alethios platform sync at onboarding
- Willing to wear Oura Ring Generation 4 continuously for 42 nights throughout the study period
- Willing to maintain stable diet, sleep habits, medications, and supplement use throughout the 42-day study period
- No planned major disruptions to sleep schedule, shift work, or travel across ≥3 time zones during the study period
- Access to a smartphone or computer to complete eConsent and digital questionnaires
- Able to provide informed consent via the Alethios eConsent platform
Exclusion Criteria:
- Current use of prescription sleep medications (benzodiazepines, non-benzodiazepine hypnotics, doxepin, suvorexant) within 30 days of enrollment
- Current use of melatonin supplements at doses >1 mg/day within 14 days of enrollment
- Diagnosis of a clinically significant sleep disorder requiring treatment (obstructive sleep apnea unless adequately treated and stable, restless legs syndrome, narcolepsy)
- Diagnosis of a major psychiatric disorder currently requiring pharmacological treatment
- Current use of hormone replacement therapy initiated within 90 days of enrollment, or any planned changes to HRT during the study (stable long-term HRT is acceptable)
- Regular use of GABAergic, serotonergic, or sedating supplements (valerian, passionflower, ashwagandha, kava) within 14 days of enrollment
- Shift work or schedule regularly requiring sleep between 06:00 and 22:00
- Planned travel across 3 or more time zones during the 42-day study period
- Known allergy to lotus, rice, or related botanicals
- Active cardiovascular, hepatic, renal, or neurological condition that in the PI's judgment would affect sleep or participant safety
- Participation in another interventional study within 30 days of enrollment
- In the opinion of the PI, any condition compromising participant safety or data integrity
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Tredobbelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: ZenRest™ Group
50 mg proprietary lotus seed and rice germ extract blend capsule, taken once daily, 30-60 minutes before bedtime for 6 weeks (42 days).
|
A proprietary blend of Lotus Seed Extract (Nelumbo nucifera) standardized to contain Neferine >/=2.0%
and Isoquercitrin & Hyperoside >/=0.5%, and Rice Germ Extract (Oryza sativa) providing Polyamines >/=0.5% calculated as spermidine.
Administered as a 50 mg capsule taken orally once daily, 30-60 minutes before bedtime, for 6 weeks (42 days).
|
|
Placebo komparator: Placebo
An identical look-alike microcrystalline cellulose capsule, taken once daily 30-60 minutes before bedtime for 6 weeks (42 days).
|
An identical, matching inactive look-alike capsule containing microcrystalline cellulose.
Administered orally once daily, 30-60 minutes before bedtime, for 6 weeks (42 days).
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Change from Baseline in Subjective Sleep Quality (PSQI Global Score) at Week 6
Tidsramme: Baseline (T0) to Week 6 (T42)
|
Evaluation of the change in the Pittsburgh Sleep Quality Index (PSQI) global summary score.
Scores range from 0 to 21, where higher scores indicate worse sleep quality and a 3-point reduction represents the minimum clinically important difference.
|
Baseline (T0) to Week 6 (T42)
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Change from Baseline in Objective Sleep Efficiency (%) via Oura Ring at Week 6
Tidsramme: Baseline Week (7-days prior to T0) and final week (T42)
|
Average weekly percentage of time spent in bed classified as sleep, calculated using nightly passive Oura Ring wearable device metrics comparing the baseline week (mean of 7 days prior to starting study product at T0) against the final week (mean of days 36-42).
|
Baseline Week (7-days prior to T0) and final week (T42)
|
|
Change from Baseline Objective Total Sleep Time at Week 6
Tidsramme: Baseline Week (7-days prior to T0) and final week (T42)
|
Total accumulated sleep duration in minutes per night, calculated using nightly passive Oura Ring wearable device metrics comparing the baseline week (mean of 7 days prior to starting study product at T0) against the final week (mean of days 36-42).
|
Baseline Week (7-days prior to T0) and final week (T42)
|
|
Change from Baseline Objective Sleep Latency at Day 42
Tidsramme: Baseline Week (7-days prior to T0) to Final Week (T42)
|
The time taken to transition from full wakefulness to sleep in minutes, calculated using nightly passive Oura Ring wearable device metrics comparing the baseline week (mean of 7 days prior to starting study product at T0) to the final week (mean of days 36-42).
|
Baseline Week (7-days prior to T0) to Final Week (T42)
|
|
Change from Baseline Objective REM Sleep Duration at Day 42
Tidsramme: Baseline week (7-days prior to T0) and final week (T42)
|
Total duration of Rapid Eye Movement (REM) sleep in minutes per night, calculated using nightly passive Oura Ring wearable device metrics comparing the baseline week (mean of 7 days prior to starting study product at T0) against the final week (mean of days 36-42).
|
Baseline week (7-days prior to T0) and final week (T42)
|
|
Change from Baseline Objective Deep Sleep Duration at Day
Tidsramme: Baseline week (7-days prior to T0) and final week (T42)
|
Total duration of Deep (slow-wave) sleep in minutes per night, calculated using nightly passive Oura Ring wearable device metrics comparing the baseline week (mean of 7 days prior to starting study product at T0) against the final week (mean of days 36-42).
|
Baseline week (7-days prior to T0) and final week (T42)
|
|
Change from Baseline Nocturnal Resting Heart Rate at Day 42
Tidsramme: Baseline week (7-days prior to T0) and final week (T42)
|
Average overnight resting heart rate in beats per minute (bpm), calculated using nightly passive Oura Ring wearable device metrics comparing the baseline week (mean of 7 days prior to starting study product at T0) against the final week (mean of days 36-42).
|
Baseline week (7-days prior to T0) and final week (T42)
|
|
Change from Baseline Nocturnal Heart Rate Variability (HRV) at Day 42
Tidsramme: Baseline Week (7-days prior to T0) to Final Week (T42)
|
Overnight Heart Rate Variability (HRV) in milliseconds (ms), calculated using nightly passive Oura Ring wearable device metrics comparing the baseline week (mean of 7 days prior to starting study product at T0) against the final week (mean of days 36-42).
|
Baseline Week (7-days prior to T0) to Final Week (T42)
|
|
Change from Baseline in Insomnia Severity Index (ISI) Total Score at Week 6
Tidsramme: Baseline (T0) to Week 6 (T42)
|
A 7-item questionnaire assessing the severity and impact of insomnia symptoms.
Total scores range from 0 to 28, where higher scores indicate greater insomnia severity.
A decrease from baseline represents an improvement.
|
Baseline (T0) to Week 6 (T42)
|
|
Change from Baseline in Epworth Sleepiness Scale (ESS) Total Score at Week 6
Tidsramme: Baseline (T0) to Week 6 (T42)
|
An 8-item questionnaire measuring a participant's general level of daytime sleepiness across daily activities.
Total scores range from 0 to 24, where higher scores indicate greater excessive daytime sleepiness.
A decrease from baseline represents an improvement.
|
Baseline (T0) to Week 6 (T42)
|
|
Change from Baseline in Health-Related Quality of Life (SF-36 Domain Scores) at Week 6
Tidsramme: Baseline (T0) to Week 6 (T42)
|
A 36-item tool measuring health status across 8 distinct domains (including vitality and mental health).
Each domain is scored from 0 to 100, where higher scores represent a better quality of life and health status.
An increase from baseline indicates an improvement.
|
Baseline (T0) to Week 6 (T42)
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Samarbejdspartnere
Efterforskere
- Ledende efterforsker: Dr. Bill Clark, PhD, Natprologix, LLC
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Anslået)
1. juli 2026
Primær færdiggørelse (Anslået)
1. september 2026
Studieafslutning (Anslået)
1. oktober 2026
Datoer for studieregistrering
Først indsendt
25. juni 2026
Først indsendt, der opfyldte QC-kriterier
25. juni 2026
Først opslået (Faktiske)
1. juli 2026
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
1. juli 2026
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
25. juni 2026
Sidst verificeret
1. juni 2026
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- NLZR-001
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
INGEN
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Ingen
Studerer et amerikansk FDA-reguleret enhedsprodukt
Ingen
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .