Effect of Rg1-based Supplementation on Exercise Training-induced Stem Cell Recruitments and Skeletal Muscle Adaptation in Women Aged > 60
Senactiv
1 other identifier
interventional
60
0 countries
N/A
Brief Summary
This study will provide novel insights into the role of bone marrow-derived stem cells in muscle adaptation to long-term exercise and advance our understanding of an Rg-1 based supplement-Senactiv® as a potential intervention for preventing sarcopenia and cognitive decline in older adults.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Aug 2026
Typical duration for not_applicable
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
July 9, 2026
CompletedFirst Posted
Study publicly available on registry
July 14, 2026
CompletedStudy Start
First participant enrolled
August 2, 2026
ExpectedPrimary Completion
Last participant's last visit for primary outcome
January 2, 2029
Study Completion
Last participant's last visit for all outcomes
January 2, 2029
July 22, 2026
July 1, 2026
2.4 years
July 9, 2026
July 20, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Bone marrow derived cells in skeletal muscle
Cell markers with bone marrow identity
* 3 weeks before exercise (baseline) * Immediately after exercise (0 hour) * 1-hour after exercise (1 h) * 24-hour after exercise (24 h)
Study Arms (2)
Placebo
PLACEBO COMPARATORSenactiv
EXPERIMENTALRg1-based supplement
Interventions
Eligibility Criteria
You may qualify if:
- \- Must be able to swallow pills
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University of Taipeilead
- Education University of Hong Kongcollaborator
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- TRIPLE
- Who Masked
- PARTICIPANT, CARE PROVIDER, OUTCOMES ASSESSOR
- Masking Details
- Care providers will administer either the placebo or the treatment to participants without knowledge of the pill centent allocation. The placebo and treatment pills will be manufactured to be indistinguishable in appearance, ensuring blinding of both care providers and participants.
- Purpose
- BASIC SCIENCE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
July 9, 2026
First Posted
July 14, 2026
Study Start (Estimated)
August 2, 2026
Primary Completion (Estimated)
January 2, 2029
Study Completion (Estimated)
January 2, 2029
Last Updated
July 22, 2026
Record last verified: 2026-07