Contemporary Clinical Trials Communications (Mar 2017)

Recruitment challenges and enrollment observations from a community based intervention (Mothers In Motion) for low-income overweight and obese women

  • Mei-Wei Chang,
  • Susan Nitzke,
  • Roger Brown,
  • M. Jean Brancheau Egan,
  • Christopher M. Bendekgey,
  • Diana Buist

DOI
https://doi.org/10.1016/j.conctc.2016.11.004
Journal volume & issue
Vol. 5, no. C
pp. 26 – 33

Abstract

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Background: Mothers In Motion (MIM), a randomized controlled trial, aimed to help young, low-income overweight and obese mothers prevent weight gain by promoting stress management, healthy eating, and physical activity. This paper describes MIM recruitment challenges and reports demographic characteristics affecting enrollment. Methods: Participants who were African American or Non-Hispanic White were recruited from the Special Supplemental Nutrition Program for Women, Infants, and Children (WIC) in Michigan. We faced numerous recruitment challenges and learned that several strategies facilitated recruitment. Logistic regression analyses were performed to examine demographic characteristics that affect enrollment. Results: Women who had a higher body mass index (BMI, OR 1.06, 95% CI 1.02–1.10); were at late postpartum, (OR 1.24, 95% CI 1.10–1.40), were breastfeeding (OR 5.0, 95% CI 2.34–10.65); or were at early postpartum and breastfeeding (OR 0.42, 95% CI 0.22–0.81) were more likely to enroll than their counterparts. Compared to African American women, Non-Hispanic White women were more likely to enroll (OR 1.77, 95% CI 1.29–2.42). Also, women who were non-smokers (OR 0.54, 95% CI 0.40–0.73) or had a higher education were more likely to enroll (OR 1.21, 95% CI 1.04–1.42) than those who smoked or had a lower education. Conclusion: Future lifestyle behavioral intervention studies for similar target audiences may consider tailoring their recruitment messages based on relevant participant demographic characteristics identified as potential determinants of enrollment in this study. Trial registration: Clinical Trials NCT01839708.

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