Does infant carrying in a soft carrier promote secure infant attachment and maternal care? A randomised controlled clinical trial
Completed
- Conditions
- eonatal DiseasesNeonatal Diseases
- Registration Number
- ISRCTN77549531
- Lead Sponsor
- Record Provided by the NHSTCT Register - 2005 Update - Department of Health (UK)
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Female
- Target Recruitment
- 0
Inclusion Criteria
Mothers of newborns that are eligible and give informed consent will be randomly assigned to the experimental or the control group, based on revealing the next in a series of random numbers.
Women who deliver a singleton live infant in the delivery suite of a large, inner-city hospital, aged 16+, accessible by telephone, able to speak conversational English, and not planning to move out of the area within 15 months will be eligible for participation in the study.
Exclusion Criteria
Not provided at time of registration
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method