Breastfeeding Clinical Trial
Official title:
The Acceptability, Feasibility, and Impact of Telelactation Among Rural Mothers
NCT number | NCT02870413 |
Other study ID # | 2016-0194-AM03 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | October 2016 |
Est. completion date | July 2018 |
Verified date | October 2019 |
Source | RAND |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The investigators will conduct a randomized controlled trial (RCT) to generate data on the impact of direct-to-consumer "telelactation" (virtual breastfeeding support) services. We will explore the feasibility, acceptability, and impact of these services. Postpartum mothers age 18 and older who have initiated breastfeeding will be recruited at a critical access hospital without access to IBCLCs in rural Pennsylvania and randomized into two study arms: 1) outpatient telelactation services via video calls on personal devices or 2) usual care. Data on breastfeeding duration and exclusivity, as well as perceptions and satisfaction with breastfeeding, will be captured via surveys and in-depth interviews and compared across groups.
Status | Completed |
Enrollment | 203 |
Est. completion date | July 2018 |
Est. primary completion date | July 2018 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 18 Years to 46 Years |
Eligibility |
Inclusion Criteria for mothers: 1. = 18 years; 2. Initiated breastfeeding while in the hospital and intend to breastfeed post-discharge 3. Fluent in English Inclusion criteria for infants: 1. Infants must be term or near term (>35 weeks gestational age) 2. Not require a stay in the neonatal intensive care unit Exclusion Criteria: 1. Prisoners, incarcerated individuals, detainees, parolees, probationers will be excluded because there may external circumstances outside of their control that may prevent continuous breastfeeding. 2. Mothers and infants will be excluded if they have maternal, fetal, or neonatal conditions or complications with the potential to physiologically compromise breastfeeding or milk supply (e.g., infant cardiac defects, post-partum infant ventilator dependence), and or contraindications to breastfeeding as specified by the American Academy of Pediatrics (e.g., HIV+ status). |
Country | Name | City | State |
---|---|---|---|
United States | RAND Corporation | Arlington | Virginia |
Lead Sponsor | Collaborator |
---|---|
RAND | University of Pittsburgh |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Any breastfeeding (yes/no) at 3 months | Three months | ||
Primary | Exclusive breastfeeding (yes/no) at 3 months | Three months | ||
Secondary | Breastfeeding satisfaction (self-reported via questionnaire at 3 months postpartum) | Survey question which captures extent of satisfaction with the experience of breastfeeding. Question reads: How satisfied do you feel about the experience of breastfeeding your baby over the past three months? (Very unsatisfied, somewhat unsatisfied, neither unsatisfied nor satisfied, somewhat satisfied, very satisfied). We will create a binary variable (satisfied vs. unsatisfied) based on this response, with those reporting "somewhat satisfied" or "very satisfied" defined as "satisfied." | Three months |
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