To Assess Effectiveness of a Nurse initiated intervention on reducing the postnatal complications.
Phase 1
- Conditions
- Health Condition 1: O758- Other specified complications of labor and delivery
- Registration Number
- CTRI/2020/06/025616
- Lead Sponsor
- ational Institute Of Nursing Education
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Closed to Recruitment of Participants
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
All antenatal mothers:-
undergoing normal
vaginal delivery
willing to participate in
the study.
Exclusion Criteria
exclusion criteria:-
Antenatal mothers
with deficits in higher
mental functions.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method It includes the variables that will be assessed during <br/ ><br>postnatal period <br/ ><br>Healing of episiotomy, <br/ ><br>Exclusive breast feeding, <br/ ><br>Absence of postnatal complications, <br/ ><br>stability of vital signs, <br/ ><br>Involution of uterus, <br/ ><br>contraceptive method adopted, <br/ ><br>Length of hospital stay. <br/ ><br>Timepoint: daily observation and recording up till discharge and at the time of postnatal follow up after 6 week period
- Secondary Outcome Measures
Name Time Method It includes the variables that will be assessed during <br/ ><br>postnatal period <br/ ><br>Healing of episiotomy, <br/ ><br>Exclusive breast feeding, <br/ ><br>Absence of postnatal complications, <br/ ><br>stability of vital signs, <br/ ><br>Involution of uterus, <br/ ><br>contraceptive method adopted, <br/ ><br>Length of hospital stay. <br/ ><br>Timepoint: daily observation and recording up till discharge and at the time of postnatal follow up after 6 week period