28 Day
28-Day Almond Milk Lactose-Reduction Trial
| STUDY TITLE | 28-Day Almond Milk Lactose-Reduction Trial |
|---|---|
| Submitted under umbrella | |
| 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 | |
| Author edit | |
| Informed consent | |
| Study author |
Gaurav PartAI |
| Principal investigator |
Matthew Amsden |
| Sub-Investigator for Adverse Events |
Dr. Viral Patel |
| Description |
Evaluate almond milk as part of a structured lactose-reduction trial to determine whether removing usual dairy milk while keeping the rest of the diet stable coincides with meaningful changes in digestive comfort, stool regularity, skin or congestion notes, and perceived quality of life. Track change through daily symptom logs, food-use tracking, and self-reported quality-of-life and energy measures. |
| Participant engagement length |
28 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 | |
| Outcome measures | |
| 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 |
| Committment to list findings on clinicaltrials.Gov |
Yes |
Preview This document is prepared with the assistance of AI, but is reviewed by a human.