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Research on Biomechanical Effects of Different Foot Landing Characteristics Based on Simulated Weightlessness

Research on Biomechanical Effects of Different Foot Landing Characteristics Based on Simulated Weightlessness

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300072662
Enrollment
Unknown
Registered
2023-06-20
Start date
2023-06-27
Completion date
Unknown
Last updated
2023-06-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

chronic disease

Interventions

1G front foot landing group :Taking the 1G gravity environment on the ground as a reference,Use pressure insoles to warn front feet of landing, analyze the differences in the characteristics of the la
1G rear foot landing group :Taking the 1G gravity environment on the ground as a reference, analyze the differences in the characteristics of hind foot landing characteristics on the mechanical effec
0G front foot landing group :Using the weightless suspension model to simulate the 0G gravity environment as a reference,Use pressure insoles to warn front feet of landing, analyze the differences in
0G rear foot landing group :Using the weightless suspension model to simulate the 0G gravity environment as a reference,Use a pressure insole to alert the rear foot to landing, analyze the difference

Sponsors

Zhengzhou University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Recruit 250 healthy volunteers with a minimum age of 18 years old; Height 165-189cm; The BMI index is between 18.5 and 23.9; Good physical health, no cardiovascular, lower limb, or foot diseases (provide recent physical examination reports), and no adverse lifestyle habits; Have a running habit in the past three months (at least 2 hours per week). Using plantar pressure insoles and high-speed cameras to record their walking, running, and jumping processes, and analyzing their foot landing characteristics. Sign an informed consent form; Those who voluntarily serve as test subjects and are able to receive treatment with experimental methods to ensure completion of the course of treatment; If other conservative treatments have been received, a washout period of at least 5 days is required. Participants in the experiment should avoid smoking, alcohol, coffee, and milk tea the day before, and maintain sufficient sleep and avoid staying up late.

Exclusion criteria

Exclusion criteria: 1. Patients under the age of 18; 2. Specific low back pain (tumor, infection, metabolic disease, rheumatoid arthritis, fracture); 3. Spinal deformity (spondylolisthesis, spondylolysis or scoliosis); 4. Pain below the knee; 5. Diseases outside the spinal cord (such as vascular and urogenital diseases); 6. Have a history of lumbar surgery; 7. There are root symptoms; 8. Low back pain with 2 or more other parts of the pain; 9. Pregnancy; 10. Patients with substantial damage to other important organs, such as severe heart, liver, kidney, lung dysfunction and cardiovascular and cerebrovascular diseases; 11. Patients prone to infection and bleeding, tumors, and postoperative dysfunction; 12. Patients who have received traditional Chinese medicine treatment such as acupuncture, massage, application and fumigation in the past 3 months; 13. Persons with previous mental illness or long-term use of sedatives; 14. Patients who cannot complete basic treatment and have poor compliance; 15. Incomplete data affect the assessment of curative effect or cannot determine curative effect; 16. Withdrawal by oneself due to adverse reactions that are difficult to tolerate. (Note: Patients meeting any of the above criteria are excluded)

Design outcomes

Primary

MeasureTime frame
Area of Center of Pressure;Fugl-Meyer Assessment Scale-lower Extremity;Functional Ambulation Category Scale;Tinetti Performance Oriented Mobility Assessment;step length;Step width;Postural stability;Barthel Index;cadence;speed;Lyscholm;Ankle joint function assessment;isual analogue scale;median frequency;joint position sense; joint kinesthesia sense;Peak torque of the flexor and extentor at different angular velocities;mean torque;Eyes closed.averagecopve locity;one leg averagecopve locity;feet together averagecopve locity;one foot in front averagecopve locity;Joint torque Angle, electromyography;VAS pain score;Joints Function Questionnaire;Gait space-time parameters;kinematic parametersduring gait;kinetic parameters during gait; Time and amplitude of EMG activation in task;Overall efficacy evaluation;Gait kinematics related parameters;Parameters related to plantar pressure;Biomechanical data;Reverse Dynamics Simulation Analysis;

Secondary

MeasureTime frame
Functional magnetic resonance;Near infrared imaging; mean power frequency;total power;articular cartilage volume; ODI score;WOMAC score;Soft tissue tension; Isorapid muscle strength test; Musculoskeletal ultrasound related parameters;maximal inspiratory muscle strength;cardiopulmonary endurance;Hamilton Anxiety Scale-14;Hamilton Depression Scale-24; The PTSD Cheklist-Civilian Version;Mindful Attention Awareness Scale;Mini Mental Status Examination;Toronto Mindfulness Scale(TMS); Multidimensional Fatigue Questionnaire; Perceived Restorative Scale(PRS);The Stanford Sleepiness Scale(SSS);Positive and negative affect scale(PANAS);Fugl-Meyer Assessment Scale;Functional Ambulation Category Scale;

Countries

China

Contacts

Public ContactPan Guo

Zhengzhou University

panguo@zzu.edu.cn+86 135 9256 1620

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026