None listed
Conditions
Interventions
Control Intervention1: NIL: NIL
Sponsors
Prerona Biswakarma
Eligibility
Inclusion criteria
Inclusion criteria: First-time mothers within the initial 12 months after childbirth, Mothers having access to healthcare, Mothers who are willing to provide informed consent to participate in the study
Exclusion criteria
Exclusion criteria: Mothers who are unwilling to provide informed consent Mothers with health complications
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 52 questions related to changes in the overall health-promoting lifestyle will be given to each participant to evaluate how daily routines and well-being are impacted before and after childbirth.Timepoint: 8 weeks | — |
Secondary
| Measure | Time frame |
|---|---|
| There are no specific intervention or endpoint criteria, as this is an observational study focused on lifestyle changes of mothers before and after childbirth. The proposed study procedures are non invasive and do not involve additional tests or interventions beyond the standard practices of the participating healthcare facilities.Timepoint: 8 weeks | — |
Countries
India
Contacts
Public ContactDr Usha Rani
Prasanna School of Public Health, MAHE
Outcome results
None listed