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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06091007
Other study ID # 5230401
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date November 17, 2023
Est. completion date June 1, 2024

Study information

Verified date December 2023
Source Loma Linda University
Contact Kyndra Woosley, MS
Phone 909-558-4000
Email kwoosley@llu.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this research study is to determine the effectiveness of magnesium on handgrip strength using the more bioavailable magnesium citrate.


Description:

In this single-blind, randomized trial, participants will take a daily dose of either 200 or 400 milligrams of magnesium citrate supplement for four weeks, perform three separate handgrip strength tests using a dynamometer, complete a demographics questionnaire, a physical activity questionnaire, and a compliance log.


Recruitment information / eligibility

Status Recruiting
Enrollment 154
Est. completion date June 1, 2024
Est. primary completion date June 1, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Generally healthy community adults - Individuals age 18 and over - Male and female participants Exclusion Criteria: - Individuals currently on magnesium supplements - Individuals currently on a multivitamin supplement - Individuals who currently suffer from hand pain or hand injury - Individuals who currently suffer from arthritis in their hands - Individuals suffering from a gastrointestinal disorder complicated by diarrhea, nausea, or abdominal cramping

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Magnesium
Magnesium citrate of either 200mg or 400 mg will be taken by the participant with food in the morning.

Locations

Country Name City State
United States Loma Linda University Loma Linda California

Sponsors (1)

Lead Sponsor Collaborator
Loma Linda University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Hand grip strength Participants will perform three separate handgrip strength tests using a Jamar Plus digital hand dynamometer, (Sammons Preston, Bolingbrook, Illinois).
In each test, participants will do three trials resting for 15 seconds between trials, the average of the three trials will be recorded. To perform the hand grip strength test, the participant will hold the dynamometer in their dominant hand, with the arm at a right angle, and with the elbow by the side of the body. The participant then squeezes the hand dynamometer with maximum isometric effort for at least five seconds. Participants are required to not move any other part of the body and are encouraged to use maximum effort.
change between baseline and 4 weeks
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