NCT07256717

Brief Summary

This prospective, multi-site, single-arm interventional study evaluates the 5-Line Principle of Balanced Progressive Intensity Training (BPIT) over 5 weeks in healthy adults aged 18-65 years. All participants receive supervised BPIT sessions (3-5 per week) progressing through five intensity lines defined by anatomical landmarks and ground reaction force: Ground-Based (Low) Knee-Level (Low-Moderate) Standing (Moderate) Head-Level (Moderate-High) Plyometric (High-Impact) The study aims to quantify improvements in functional movement efficiency, joint mobility, postural control, strength adaptation, and heart-rate variability while monitoring safety and individual overload indicators.

Trial Health

60
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
369

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Oct 2025

Shorter than P25 for not_applicable

Geographic Reach
2 countries

10 active sites

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

October 10, 2025

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

November 18, 2025

Completed
13 days until next milestone

First Posted

Study publicly available on registry

December 1, 2025

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 15, 2026

Completed
10 days until next milestone

Study Completion

Last participant's last visit for all outcomes

February 25, 2026

Completed
Last Updated

December 16, 2025

Status Verified

December 1, 2025

Enrollment Period

4 months

First QC Date

November 18, 2025

Last Update Submit

December 8, 2025

Conditions

Keywords

Balanced Progressive Intensity TrainingBPIT5-Line PrincipleMovement EfficiencyHeart Rate VariabilityPostural ControlStrength TrainingExercise InterventionNeuromuscular Adaptation

Outcome Measures

Primary Outcomes (1)

  • Movement Efficiency Score (MES, 0-10)

    Change from baseline in the proprietary Movement Efficiency Score (MES), a validated composite metric of biomechanical function, movement quality, and postural alignment (derived from MMSx Flaw Checklist, visual/video analysis, and functional mapping).

    Baseline (Week 0) and end of study (Week 5)

Secondary Outcomes (4)

  • Range of Motion (ROM)

    Baseline and Week 5

  • VAS Pain Score

    Baseline and Week 5

  • Strength Index

    Baseline and Week 5

  • Mobility Limitation (%)

    Baseline and Week 5

Other Outcomes (1)

  • Heart Rate Variability (HRV - RMSSD)

    Baseline and Week 5

Study Arms (1)

BPIT 5-Line Training Group

EXPERIMENTAL

All participants receive the 5-week Balanced Progressive Intensity Training (BPIT) program using the 5-Line Principle (ground-based → knee-level → standing → head-level → plyometric) under supervised sessions 3-5 times per week.

Behavioral: Balanced Progressive Intensity Training (BPIT) 5-Line Method

Interventions

5-week supervised progressive training using the BPIT 5-Line framework developed by Dr. Neeraj Mehta.

BPIT 5-Line Training Group

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Adults aged 18-65 years Generally healthy with regular physical activity history (at least 1-2 sessions per week for the past 3 months) Able to commit to 3-5 supervised training sessions per week for 5 weeks Willing and able to provide written informed consent Cleared by pre-screening (no acute injury, no contraindications)

You may not qualify if:

  • Acute musculoskeletal injury within the past 3 months Known cardiovascular, metabolic, or orthopaedic conditions that contraindicate exercise Pregnancy or planning pregnancy Use of medications or supplements that significantly affect muscle recovery or performance (e.g., corticosteroids, anabolic agents) Inability to follow the BPIT protocol or attend required sessions

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (10)

BodyGNTX Fitness Institute

Columbus, Ohio, 43220, United States

RECRUITING

MMSx Authority Biomechanics Department

Powell, Ohio, 43065, United States

RECRUITING

MMSx AUTHORITY INSTITUTE FOR MOVEMENT MECHANICS & BIOMECHANICS RESEARCH (COORDINATING CENTER)

Powell, Ohio, 43065, United States

RECRUITING

Indian Institute of Kinesiology & Biomechanics Science (IIKBS)

Burhānpur, Madhya Pradesh, 450331, India

RECRUITING

Shri Mahaveer Ortho Clinic

Delhi, National Capital Territory of Delhi, 110032, India

RECRUITING

GFFI Fitness Academy

New Delhi, National Capital Territory of Delhi, 110026, India

RECRUITING

Active India Health & Fitness Trust (AIHFT)

New Delhi, National Capital Territory of Delhi, 110063, India

RECRUITING

Body Mechanics Gym P Ltd

New Delhi, National Capital Territory of Delhi, 110092, India

RECRUITING

Regain Fitness Zone

Greater Noida, Uttar Pardesh, 201310, India

RECRUITING

GFFI Fitness Academy

Agra, Uttar Pradesh, 282005, India

RECRUITING

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Masking Details
Single-arm prospective interventional study
Purpose
OTHER
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

November 18, 2025

First Posted

December 1, 2025

Study Start

October 10, 2025

Primary Completion

February 15, 2026

Study Completion

February 25, 2026

Last Updated

December 16, 2025

Record last verified: 2025-12

Data Sharing

IPD Sharing
Will not share

Locations