Assessment of the feasibility of Juntos: A support programme for families of children affected by Congenital Zika Syndrome
Open Access
- 4 March 2022
- journal article
- research article
- Published by F1000 Research Ltd in Wellcome Open Research
- Vol. 7, 77
Abstract
Background: The 2015-16 Zika epidemic resulted in thousands of children born with congenital Zika syndrome (CZS). In Brazil, gaps in the health system often caused parents to be left with insufficient information and support. Consequently, we developed and piloted Juntos - a participatory support programme which aims to improve knowledge, capacities and build support networks for caregivers of children with CZS. Methods: Six caregiver groups received the programme between August 2017 and June 2018: three in Rio de Janeiro and three in Bahia. We assessed the feasibility of Juntos against six of the eight areas of a feasibility framework described by Bowen et al. to consider whether Juntos ‘could work’. These areas were: acceptability, demand, implementation, practicality, adaptation and limited efficacy. We used mixed methods including: 1) baseline and end-line questionnaires completed by all group participants; 2) in-depth interviews with 18 participants, seven facilitators and three key stakeholders; 3) participant focus group discussions after each session; 4) researchers session observation; and 5) recording programme costs. Results: 37/48 (77%) enrolled families completed both questionnaires. Acceptability and demand were noted as high, based on participant responses to interview questions, focus group feedback and satisfaction scores. Potential for implementation and practicality were also demonstrated through interviews with facilitators and key stakeholders and analysis of project documents. Two groups included caregivers of children with non-Zika related developmental disabilities, showing potential for adaptability. Self-reported quality of life scores increased in caregivers between baseline and end-line, as did the dimensions of family relationships and daily activities in the Pediatric Quality of Life Inventory (PEDS QL) Family Impact Module, showing limited efficacy. Conclusions: The programme showed feasibility according to Bowen’s framework. However, further research of scale up, particularly in the areas of integration, expansion and limited efficacy are needed to ascertain if the programme is effective.Keywords
Funding Information
- Wellcome Trust (206719)
- Wellcome Trust (212156)
This publication has 23 references indexed in Scilit:
- Development of Infants With Congenital Zika Syndrome: What Do We Know and What Can We Expect?Pediatrics, 2018
- The Zika Virus Epidemic in Brazil: From Discovery to Future ImplicationsInternational Journal of Environmental Research and Public Health, 2018
- Anxiety, depression, and quality of life in mothers of newborns with microcephaly and presumed congenital Zika virus infection: a follow-up study during the first year after birthArchives of Women's Mental Health, 2017
- Characterizing the Pattern of Anomalies in Congenital Zika Syndrome for Pediatric CliniciansJAMA Pediatrics, 2017
- Zika Virus and Birth Defects — Reviewing the Evidence for CausalityNew England Journal of Medicine, 2016
- Functional priorities reported by parents of children with cerebral palsy: contribution to the pediatric rehabilitation processBrazilian Journal of Physical Therapy, 2014
- How We Design Feasibility StudiesAmerican Journal of Preventive Medicine, 2009
- The Pediatric Quality of Life Inventory™ (PedsQL™) family impact module: reliability and validity of the Brazilian versionHealth and Quality of Life Outcomes, 2008
- Predictors of Stress in Mothers of Children With Cerebral Palsy in BangladeshJournal of Pediatric Psychology, 2000
- The PedsQL™: Measurement Model for the Pediatric Quality of Life InventoryMedical Care, 1999