Clinical TrialID 8165

Creatine Supplementation and Resistance Training in Premenopausal Females

NCT05745870

Health Behavior

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Record Fields

Scalar fields from the final clinical_trial record.

Clinical Trial Id
8165
Evidence Id
8165
Core Evidence Id
8165
Source Clinical Trial Id
8163
Herb2 Clinical Trial Id
HBCT008163
Nct Id
NCT05745870
Title
Creatine Supplementation and Resistance Training in Premenopausal Females
Status
Completed
Phase
Phase 1
Study Result
No
Study Condition
Health Behavior
Study Type
Interventional
Study Design
Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: DOUBLE (PARTICIPANT, INVESTIGATOR)|Primary Purpose: TREATMENT
Intervention
DIETARY_SUPPLEMENT: Creatine Monohydrate Supplementation
Intervention Allocation
Randomized
Intervention Model
Parallel
Intervention Mask
Double
Intervention Purpose
Treatment
Gender
Female
Age
Adult
Enrollment
27
Outcome Measure
Body Composition, Change in lean mass (kg, %) using a DXA scan from baseline after 42 days, 42 days|Sleep, Change in sleep (hours, minutes, REM) using the Oura Ring application tracking from baseline after 42 days, 42 days|Muscular Strength, Change in muscular strength (1-repetition maximum) using the Tonal from baseline after 42 days, 42 days|Perceived Menstrual Cycle Symptoms, Change in perceived menstrual cycle symptoms (fatigue, cramping, bloating) using menstrual cycle questionnaires from baseline after 42 days, 42 days
Sponsor Collaborator
University of Idaho
Funded By
OTHER
Location
University of Idaho, Moscow, Idaho, 83844, United States
Other Id
21-170
Start Date
2023-01-20
Primary Completion Date
2023-05-12
Completion Date
2023-05-12
First Posted
2023-02-27
Results First Posted
Last Update Posted
2023-09-07
Study Document
Study Url
https://clinicaltrials.gov/study/NCT05745870
Title Cn
Title En
Creatine Supplementation and Resistance Training in Premenopausal Females
Bilingual Status
semi_complete