Effectiveness of shortened time interval to postpartum visit in improving postpartum attendance: Design and rationale for a randomized controlled trial
Autor: | Nicole W. Karjane, Whitney C Graves, Gloria J. Bazzoli, Timothy O. Ihongbe, Wen Wan, Saba W. Masho, Pamela Dillon, Elizabeth A. McGee |
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Rok vydání: | 2019 |
Předmět: |
Adult
medicine.medical_specialty Time Factors Adolescent law.invention Appointments and Schedules Young Adult 03 medical and health sciences 0302 clinical medicine Randomized controlled trial law medicine Humans Pharmacology (medical) University medical Prospective Studies 030212 general & internal medicine 030505 public health business.industry Postpartum Period Attendance General Medicine Research Design Physical therapy Patient Compliance Female 0305 other medical science business |
Zdroj: | Contemporary Clinical Trials. 81:40-43 |
ISSN: | 1551-7144 |
DOI: | 10.1016/j.cct.2019.04.012 |
Popis: | Background/Aims Recent evidence suggests that there are numerous benefits to scheduling postpartum visits as early as 3 weeks post-delivery. However, findings are not conclusive due to methodological limitations. This report discusses the unique aspects of a randomized controlled trial's (RCT) design, intervention, and strategies to maintain participant retention. Methods This study was a four-year, prospective, open-label RCT conducted at the Virginia Commonwealth University Medical Center. Women who recently delivered a healthy, full-term baby vaginally, were randomized to receive a 3–4 or 6–8 weeks postpartum appointment and were followed for 18 months. Results A total of 364 women participated in this study. A large proportion of women were retained in the study as demonstrated by the high completion rates at the 18-month follow-up interview (Total sample: 87.6%; 3–4 weeks group: 88.0%; 6–8 weeks group: 87.3%). Similarly, high adherence to the protocol-directed postpartum visit schedule was reported in the overall study sample (79.7%), as well as in the 3–4 (70.5%) and 6–8 (90.0%) week postpartum groups. Conclusion The study design offered unique features which ensured excellent participant completion and adherence rates, despite the presence of hard-to-track women who typically do not return for their postpartum visits. |
Databáze: | OpenAIRE |
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