Health Condition 1: K590- Constipation Health Condition 2: N946- Dysmenorrhea, unspecified Health Condition 3: J453- Mild persistent asthma Health Condition 4: M179- Osteoarthritis of knee, unspecified
Conditions
Interventions
None listed
Sponsors
Central Council for Research in Ayurvedic Sciences
Eligibility
Inclusion criteria
Inclusion criteria: For CABHA :Eligibility Assessment for participation in the survey – 1) Of age =18 years 2) Able to respond or communicate 3) Willing to participate in the survey For IAHA (Applicable only on Cluster -1) The families residing in the identified areas and consisting of at least 2 members and, at least one among them is aged =18 years • At least one adult member in the family is willing to participate in this study for the 4 months
Exclusion criteria
Exclusion criteria: 1) The families those are planning to move out of the identified area during the study period. 2) Families whose members cannot dedicate any suitable time for the activities involved in this study (personal interview and counseling) 3) Head of the family does not consent for participation of any member
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Any change in perception & health-seeking behavior of the selected population after introduction of the CABHATimepoint: To be assessed through a questionnaire administered among the randomly selected sample for survey in two clusters, before and after the interventions(4 months) in the community | — |
Secondary
| Measure | Time frame |
|---|---|
| 1.Any change in the score of quality of life (SF-12) of the surveyed participants (including selected families) 2. Any change in the score of Immune Status Questionnaire (ISQ) in the participants from the included families 3.Any change in WHO-5 Wellbeing Index score of the participants from the included families 4.Any change in the score of Global Sleep Assessment Questionnaire (GSAQ) of the participants from the included families 5.Any change in the Oral Health Assessment Tool (OHAT) score of the participants from the included families 6.Any change in the scores of disease specific patient reported outcomes of the participants in the community (including selected families) 7.Proportion of participants adhering (=60%) to the Ayurveda advocacy and/or treatment throughout the duration of intervention 8.Trend in rise of OPD attendance in the outreach OPDs during the intervention periodTimepoint: 1.to be assessed during baseline & end-line surveys 2.to be assessed at baseline, 60th day & 120th day 3.to be assessed at baseline, 30th day, 60th & 90th day 4.to be assessed at baseline, 60th day & 120th day 5.to be assessed at baseline, 60th day & 120th day 6.(Acute conditions: to be assessed at baseline, & as per the course of disease) 7.to be assessed at baseline, 30th day, 60th, 90th & 120th day. 8.4 months | — |
Countries
India
Contacts
Public ContactDr Sunita
Central Council for Research in Ayurvedic Sciences
Outcome results
None listed