4.5 Article

Applying the RE-AIM framework to evaluate the implementation of the Supporting and Enhancing NICU Sensory Experiences (SENSE) program

Journal

BMC PEDIATRICS
Volume 21, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s12887-021-02594-3

Keywords

Parent; Environment; Therapy; Outcomes; Fidelity; Preterm; Reach; Effectiveness; Adoptability; Maintenance

Categories

Funding

  1. Gordon and Betty Moore Foundation
  2. Washington University Institute of Clinical and Translational Sciences from the National Center for Advancing Translational Science, Institute of Health [UL1TR002345, RO1 HD 057098]
  3. Intellectual and Developmental Disabilities Research Center at Washington University (NIH/National Institute of Child Health and Human Development) [P30 HD062171]

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The SENSE program, implemented in the NICU, showed good reach, effectiveness, and acceptability. Parent participation was influenced by early education.
BackgroundTo maximize the benefit of parent-directed, positive sensory exposures in the NICU, a structured sensory-based program titled the Supporting and Enhancing NICU Sensory Experiences (SENSE) program was developed that includes specific doses and targeted timing of evidence-based sensory exposures.MethodsThe Reach, Effectiveness, Adoption, Implementation, Maintenance (RE-AIM) framework was used to systematically evaluate the SENSE program as an implementation strategy. One-hundred preterm infants <= 32weeks gestation were studied (61 receiving the SENSE program and 39 standard-of-care). Parent education time and infant sensory exposures were tracked, and parents completed a questionnaire that probed their perceptions about the SENSE program.ResultsOne-hundered thirty-one families were recruited, and 100 (76%) enrolled. The SENSE program was initiated at an average postmenstrual age of 29.8 (2.4) weeks; 4.9 (+/- 5.6) days after birth. The average number of education sessions with families was 4.8 (+/- 3.7) amounting to 72.3 (+/- 37.4) total minutes over hospitalization. The total time of logged tactile and auditory exposures among SENSE recipients over the length of hospitalization was a median (IQ range) of 9325 (5295-15,694) minutes over an average of 10.1 (+/- 7.6) weeks of hospitalization. There were differences in the proportion of tactile and auditory exposure targets received by the infant among those receiving the SENSE program compared to standard-of-care (91% compared to 48%; p <0.0001). Ninety-five percent of infants tolerated the SENSE program as defined, with 5% of infants requiring intermittent adaptations or the interventions being stopped for a period that typically lasted 1-2weeks. Earlier parent education was related to more parent participation in SENSE program interventions (p =0.04). Eighty-five percent of participants receiving the SENSE program had most of the sensory interventions completed by parents, as opposed to the medical or sensory support team. Seventy-two percent of infants had at least 100% of the auditory and tactile doses conducted over the length of stay. Parents reported acceptability.Conclusion The SENSE program had good reach, was effective and acceptable with minimal cost, was adopted, and had good fidelity. Insights from implementation of the SENSE program (within a research study) informed future strategies to aid maintenance during dissemination.

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