Evaluating a Coparenting Breastfeeding Support Intervention (COSI)
The purpose of this trial is to evaluate the effectiveness of a Coparenting Breastfeeding Support Intervention with first time parents on exclusive breastfeeding rates at 12 weeks postpartum. Partner support and the coparenting relationship will also be evaluated.
Behavioral: Coparenting Breastfeeding Support Intervention
|Study Design:||Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single Blind (Outcomes Assessor)
Primary Purpose: Treatment
|Official Title:||Evaluating the Effectiveness of a Coparenting Breastfeeding Support Intervention on Exclusive Breastfeeding Rates at 12 Weeks Postpartum|
- Exclusive Breastfeeding rate at 12 weeks postpartum [ Time Frame: 12 weeks postpartum ] [ Designated as safety issue: No ]Exclusive breastfeeding will be determined by asking the mother what she has fed her baby in the last 24 hrs. This is consistent with the World Health Organizations definition of exclusive breastfeeding and full breastfeeding described by Labbok and Krasovec (1990). This is defined as no food or liquid other than breast milk given to the infant; however, undiluted drops or syrups consisting of vitamins, minerals supplements or medicines are included (Breastfeeding Committee for Canada, 2006; WHO, 2010).
- Coparenting Relationship [ Time Frame: 6 & 12 weeks postpartum ] [ Designated as safety issue: No ]Coparenting is the degree to which parents work together to achieve parenting goals. This will be measured using Feinberg, Brown and Kan (2010) Coparenting Relationship Scale (CRS). There are 35 items in total in this tool.
- Breastfeeding Support [ Time Frame: 6 & 12 weeks ] [ Designated as safety issue: No ]Breastfeeding support is defined as the appraisal, emotional, informational and instrumental support the mother recieves from her partner. This component of coparenting will be measured using the Postpartum Partner Support Scale (PPSS), which is a 24-item self-report instrument.
- Breastfeeding Duration [ Time Frame: 6 & 12 weeks ] [ Designated as safety issue: No ]Breastfeeding duration is defined as the length of time in which the infant receives breast milk. The degree of breastfeeding will be measured using the schema and framework developed by Labbock and Krasovec (1990) for defining breastfeeding.
|Study Start Date:||February 2012|
|Estimated Study Completion Date:||January 2013|
|Estimated Primary Completion Date:||October 2012 (Final data collection date for primary outcome measure)|
Experimental: Coparenting Breastfeeding Support Intervention
The intervention group will receive a in-hospital discussion, a video, workbook, breastfeeding booklet, access to a secure study website and two follow-up phone calls
Behavioral: Coparenting Breastfeeding Support Intervention
The intervention group will receive standard care offered to breastfeeding women in the hospital and community with the addition of a multifaceted coparenting breastfeeding support intervention, which will include an in hospital discussion, a video, workbook, breastfeeding booklet, and access to a secure website. Additionally, two follow-up phone calls will be made at 1 and 4 weeks postpartum. This intervention has been designed with coparenting elements and contains extensive breastfeeding information.
No Intervention: Usual Care Group
The usual care group will receive standard postpartum care in the hospital and in the community
Breastfeeding is the recommended infant feeding method by leading health authorities. This recommendation is based on the many health benefits breastfeeding provides to both women and their infants. Breastfeeding rates in Canada, however, are suboptimal, with nearly half of mothers discontinuing exclusive breastfeeding in the first three months and less than twenty-five percent of mothers meeting the recommendation of exclusive breastfeeding to six months.
There are many factors associated with the premature cessation of exclusive breastfeeding. They include demographic, biological, psychosocial, and social factors. Some of these factors are not modifiable, such as age, social status, and education level, as they are not amenable to an intervention. One possible modifiable factor, which may assist women in overcoming breastfeeding difficulties, is fathers' support with breastfeeding. Fathers' favourable attitude and support of breastfeeding positively impacts breastfeeding initiation, duration, and exclusivity. Research on ways to assist fathers in providing support for breastfeeding is needed. The ways in which fathers can provide effective support can best be determined through intervention studies designed to increase fathers' supportive behaviour towards breastfeeding. Specifically, a coparenting framework to guide such interventions would be optimal as coparenting teaches parents to work in partnership towards positive child health outcomes. The purpose of this proposed randomized controlled trial is to evaluate the effects of a coparenting breastfeeding support intervention, delivered to primiparous breastfeeding mothers and the infants' fathers (the breastfeeding woman's male partner, who is jointly responsible for the child). It is hypothesized that this intervention will increase exclusive breastfeeding at 12 weeks postpartum. The secondary outcomes will be breastfeeding duration, perceived breastfeeding support, and coparenting at 6 and 12 weeks.
Participants will include first-time breastfeeding women and the infants' fathers who have singleton births and full term healthy infants. Eligible parents who consent to participate will be randomized into either the intervention group or the control group. The control group will receive standard postpartum care, which is routine care in the hospital and community related to breastfeeding. The intervention group will receive standard postpartum care, plus a multifaceted support intervention that includes: (1) a professional-based in-hospital visit in the first two days postpartum that uses a take-home workbook and video, (2) one or two follow-up phone calls in the first and fourth week postpartum, and (3) access to a secure study website for a three month period. All of the components in this intervention will contain extensive information on coparenting and breastfeeding. Follow-up data will be collected by the method chosen by participants, either by web-based survey or telephone interview. This data will be collected by a research assistant blinded to group allocation and data collection points will be at 6 and 12 week postpartum.
The results of this study will be of interest to health care professionals who work with breastfeeding women and their families, as well as policy makers designing programs to meet the needs of childbearing families.
|Contact: Jennifer M Abbass Dick, PhD (C)||email@example.com|
|Contact: Cindy-Lee Dennis, PhDfirstname.lastname@example.org|
|North York General Hospital||Not yet recruiting|
|North York, Ontario, Canada, M2K 1E1|
|Principal Investigator:||Cindy-Lee Dennis, PhD||University of Toronto|