§ 01

Registered Clinical Investigations

MMSx Authority conducts registered clinical investigations aligned with international ethical and research standards. All interventional studies are pre-registered on ClinicalTrials.gov prior to data collection, and conducted under GCP ICH E6(R3) and the Declaration of Helsinki (2013). Each record below links to its public ClinicalTrials.gov entry, where current recruitment status and the full protocol can be verified.

§ 02

Study Registry — ClinicalTrials.gov

StudyNCT RegistrationDesignPlanned nSitesStatus
MOVE Protocol
Movement-Oriented Velocity of Engagement
NCT07220200 Multi-site interventional case-series · 8-week · 4-phase 40 GFFI New Delhi · BodyGNTX USA · IIKBS Registered · Results pending
BPIT Pilot Study
5-Line Principle — Strength, HRV & Injury Risk
NCT07296640 Prospective single-site · Paired t-tests α=0.05 · Cohen's d 23 BodyGNTX USA Registered · Results pending
BPIT Multi-Site Study
International Multi-Site Evaluation
NCT07256717 Multi-site single-arm interventional · 5 sites · Mixed-effects ANOVA 369 BodyGNTX · GFFI · IIKBS · AIHFT · BFS Registered · Recruiting
§ 03

Pre-Specified Outcomes by Study

NCT07220200 · MOVE Protocol
MOVE Protocol — Outcomes

Pre-specified outcomes: pain indices, functional capacity, balance performance, and sit-to-stand metrics across sites in India and the USA. The full protocol is publicly available on ClinicalTrials.gov. Results to be reported on completion.

NCT07296640 · BPIT Pilot
BPIT Pilot — Outcomes

Pre-specified outcomes: strength, heart-rate variability, and knee-valgus loading, with a pre-registered statistical analysis plan. Framework archived on Zenodo (DOI 10.5281/zenodo.17594977). Results to be reported on completion.

NCT07256717 · BPIT Multi-Site
Multi-Site Study — Outcomes

Pre-specified outcomes: strength, heart-rate variability, and injury-mitigation measures across five international sites, designed to assess cross-site reproducibility. Protocol/preprint archived on Zenodo (DOI 10.5281/zenodo.17551763). Results to be reported on completion.

§ 04

Ethics & Compliance

  • GCP ICH E6(R3) — Good Clinical Practice guidelines for all registered investigations
  • Declaration of Helsinki (2013 revision) — ethical principles for human subjects research
  • Pre-registered Statistical Analysis Plans (SAPs) locked before data collection begins
  • Independent statistician verification of primary analyses
  • Open datasets archived on OSF and Zenodo (CC BY 4.0) for independent verification
  • Conflict of interest disclosure on all publications
→ Full Ethics & Governance documentation
Disclaimer: Content is provided for scientific and educational purposes only. It does not constitute medical advice, diagnosis, or treatment. Clinical decisions must remain the responsibility of licensed healthcare professionals.