To assess the decrease in pain in neonates during painful procedures by making the mothers to hold their newborns, without using pain-relieving medications.
Phase 1
- Conditions
- Health Condition 1: G891- Acute pain, not elsewhere classified
- Registration Number
- CTRI/2023/08/056592
- Lead Sponsor
- Post Graduate Institute of Medical Education and Research
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
All preterm neonates more than and equal to 35 weeks of the gestation age.
Exclusion Criteria
1.Neonates who will be in shock.
2.Critically ill neonates.
3. Neonates who will be on sedative analgesics.
4. Neonates who will be getting drugs like morphine, midazolam which can cause CNS depression.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The level of pain will be decreased with facilitated tucking provided by mothers to their preterm neonates during selected procedures.Timepoint: 2 weeks after intervention.
- Secondary Outcome Measures
Name Time Method The anxiety & stress level of mothers of the preterm neonates will be decreased when they will be participating in providing facilitated tucking during selected painful procedures.Timepoint: Stress & anxiety level of mothers of the preterm neonates will be checked after the selected painful procedures.;The stress & anxiety of mothers of the preterm neonates will be decreased when they will be participating in providing facilitated tucking during selected painful procedures.Timepoint: Stress & anxiety levels of mothers of the preterm neonates will be checked after the selected painful procedures.