None listed
Conditions
Interventions
Intervention1: Arnica Montana
: 30CH homoeopathic preparation
Three 8 hourly doses preferably before meal for 3 days.
Control Intervention1: Placebo: Dosing schedule as per Intervention
Sponsors
Central Council for Research in Homoeopathy
Eligibility
Inclusion criteria
Inclusion criteria: Subjects will be the normal, healthy, non-athletic graduate/post graduate/male/female students.
Exclusion criteria
Exclusion criteria: Subjects suffering from any disorder of hand, wrist, upper limb, and neck will be excluded. These disorders include, but are not limited to, tendonitis trigger finger, De Quervain?s disease, carpel tunnel syndrome, and tennis elbow, arthritis of small joints of hand, cervical spondylosis, and injuries of hand, wrist and upper limb.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Physiological monitoring of induction of muscle fatigue under the guidance of physiologist and detection of Maximum Voluntary Contraction for every individual participant. 2. Noninvasive objective assessment for identification of muscle fatigue using Electromyography (EMG), Photoplethysmography (PPG), Impedance plethysmography (IPG). 3. Scientific validation of induced muscle fatigueTimepoint: 1 to 12 weeks | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Technology will be developed for identification of muscle fatigue Instrument modifications for objective assessment using online Signals processing. 2. Study may establish Arnica Montana as muscle tonic. 3. Ultra high molecular dilutions can alter physiological signals. Timepoint: 1 to 12 weeks | — |
Countries
India
Contacts
Public ContactHARI SINGH
AIIMS AND IIT DELHI
Outcome results
None listed