None listed
Conditions
Interventions
Intervention1: Indicated homoeopathic medicines: Known pharmacopoeial preparations in various potencies and dosage as per the disease condition (acute/ chronic) and discretion of the physician. Time p
Sponsors
Central Council for Research in Homoeopathy
Eligibility
Inclusion criteria
Inclusion criteria: Participants employed on part-time/full time basis at tea gardens Participants who shall give a written informed consent
Exclusion criteria
Exclusion criteria: Refusal of consent by the participant Pregnant and lactating women
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Burden of morbidities and symptoms 2. Duration, intensity of symptoms 3. Improvement on outcome rating scalesTimepoint: For 1 at baseline For 2 Daily, weekly, fortnightly or monthly depending on the condition For 3 Baseline , every 3-6 months | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Use of conventional medicines including antibiotics in the targeted population 2. Changes in Quality of life 3. Days of hospitalisation 4. Loss of workdays and loss of incomeTimepoint: For 1, 3, 4 Each episode For 2 Baseline, 6, 12 months | — |
Countries
India
Contacts
Public ContactDr Amulya Ratan Sahoo
Central Council for Research in Homoeopathy, New Delhi, Ministry of AYUSH, Govt. of. India
Outcome results
None listed