Viewing Study NCT06499012



Ignite Creation Date: 2024-07-17 @ 11:16 AM
Last Modification Date: 2024-10-26 @ 3:34 PM
Study NCT ID: NCT06499012
Status: NOT_YET_RECRUITING
Last Update Posted: 2024-07-12
First Post: 2024-07-06

Brief Title: The Efficacy of Nutrilite All-plant Protein Booster to Improve Sarcopenia and Osteoarthritis in Middle-aged and Elderly People
Sponsor: Amway China RD Center
Organization: Amway China RD Center

Study Overview

Official Title: A Randomized Double-blind Clinical Study of the Efficacy of Nutrilite All-plant Protein Booster to Improve Sarcopenia and Osteoarthritis in Middle-aged and Elderly People
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-07
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The goal of this clinical trial is to learn whether Amway Nutrilite All-plant protein booster prototype product test product will improve sarcopenia SA and osteoarthritis OA in middle-aged and elderly people It will also learn about the improvement of Quality of life QoL in them The main questions it aims to answer are

Does the test product will improve the SA in terms of Short Physical Performance Battery SPPB score after 12 weeks intervention
Does the test product will improve the OA in terms of Western Ontario and McMaster Universities Arthritis WOMAC Index after 12 weeks intervention

Researchers will compare Amway All-plant protein booster prototype product to a placebo a look-alike substance that contains no similar active nutrient ingredients to see if the test product works to improve SA and OA

Participants will

Take the test product or a placebo 2 spoons 15g twice per day for 12 weeks
Visit the site on the baseline day and the 84th day end day of 12 weeks for checkups and tests
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None