29 Day

After-7 PM Late Snack Sleep Trial

STUDY TITLE After-7 PM Late Snack Sleep Trial
Submitted under umbrella

Umbrella Protocol for Efforia Personalized Agentic Hypothesis Discovery & Experiential Proof Trials

Date submitted

—

End date

There is no pre-specified end date and sub-studies remain open long-term.

Language

English

Efforia AI IRB approval recommendation

—

Recruitment page preview

Preview

Informed consent

Review

Study author

Alex Zelvin

Principal investigator

Matthew Amsden

Sub-Investigator for Adverse Events

Dr. Viral Patel

Description

This draft uses a within-person alternating-day eating-timing routine to compare early evening cutoff days with late-snack days. Participants complete all caloric intake by 7:00 pm on early-cutoff days and consume one normal late snack after 7:00 pm on late-snack days. The protocol prioritizes real-world usefulness while keeping the timing rule clear and consistent across the full alternating schedule.

Participant engagement length

29 Days

Sponsor

This study is made possible by your payment to cover all supplies and expenses required to participate.

Cost to participant

$0

Included products & services
Oura Ring: $0
Outcome measures

Oura Sleep

Methodology

Single Arm longitudinal where participants act as their own control

Basic or advanced dissemination plan

Basic

Deviation from recruitment approach

No

Deviation from statistical approach

No

Will study include “more about you questions”

No

ClinicalTrials.gov

Yes

Commitment to list findings on ClinicalTrials.gov

Yes

This document is prepared with the assistance of AI, but is reviewed by a human.

Rational & Study Design

Reason I Created This Protocol:

Late eating is blamed for restless nights, groggy mornings, and “bad recovery,” while social feeds swear an after-dark bite can either wreck sleep or save it. Research links meal timing with circadian biology, glucose patterns, and sleep quality, but real-world late snacking data are messy. This study tests the midnight-munch folklore with a clean 7 pm line, wearable sleep metrics, and you as your own control.

My Objective For You:

To help you determine whether one normal snack after 7 pm meaningfully shifts your personal sleep patterns versus finishing calories by 7 pm, using alternating days and wearable sleep data from baseline through Day 31. By the end, you should see your own signal—not generic wellness gossip—so you can decide if late snacking earns a spot in your evening routine.

Aims & Objectives:

This protocol compares early evening calorie cutoff days with late-snack days to evaluate changes in sleep patterns across a practical 31-day self-experiment. You will receive personalized results showing how this timing rule affects your nights and mornings, helping you make smarter decisions about your food routine, recovery habits, time, and money.

Significance & Impact:

Late-night snacking is a common behavior with plenty of opinion and less personal proof. This study may clarify whether snack timing influences your sleep and recovery patterns in daily life, while recognizing limitations such as self-selection, imperfect dietary control, normal life stress, and wearable-derived rather than laboratory sleep measures. It is for health optimization and self-learning, not diagnosis or treatment.

The Intervention

Included Products & Services

Product Name: Oura Ring

Quantity included: 1

Price: $0.00

Product Description:

The Oura Ring is a piece of wearable technology designed to help you understand your body and improve your overall health. It is a small, lightweight ring that captures data from your body 24/7 and provides insights into your sleep, activity, and readiness. It is designed to be comfortable and discreet, and is made of hypoallergenic materials. The Oura Ring is a powerful tool that helps you to understand your body and make meaningful changes to your lifestyle.

Product Image: —

Ingredients:

Product Safety:

Study Design & Methodology

Inappropriate Participants & Inclusion/Exclusion

Study Design & Experience

Statistical Analysis Plan

Limitations & Justification

Human Subjects Ethics

Suitability Under Minimal Risk Umbrella Protocol

Suitability for Pay to Participate Model

Human Subjects Protection Questionnaire