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December 8, 2025Blood

The feasibility of collecting social determinants of health in the national multi-center GRASP sickle cell gene therapy trial

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Authors

WLWendy B. LondonNorthwestern UniversityVCVictoria H. Coleman‐CowgerEmmes (United States)
Mary M. Horowitz
Mary M. HorowitzNorthwestern University

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Overview

Clinical trial assesses the feasibility of collecting social determinants of health data in sickle cell gene therapy, highlighting poverty's impact on outcomes.

Key Points

  • To evaluate the feasibility of collecting poverty-related data in a multi-center gene therapy trial for sickle cell disease.
  • Phase II, single-arm trial involving patients aged 13-40 with clinically severe sickle cell disease.
  • Patients completed a 21-item Household Survey at baseline and 24-month follow-up.
  • Data collection monitored centrally, with surveys available in multiple languages.
  • Primary exposure of interest was household material hardship, including food and housing insecurity.
  • 100% of participants completed the baseline Household Survey across 8 sites.
  • All surveys had evaluable household material hardship data.
  • 38% of participants reported exposure to household material hardships, mainly food and housing insecurity.

Cite This Study

London et al. (2025) studied this question.

synapsesocial.com/papers/69362f3d4fa91c937236d53bhttps://doi.org/10.1182/blood-2025-6224
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Household material hardship as a barrier to accessing sickle cell disease curative therapy2025
  2. 2Out of Reach: Understanding Resource Barriers to Gene Therapy for Pediatric Patients With Sickle Cell Disease2026
  3. 3Prospective observational cohort study to collect granular social determinants of health data for hematopoietic cell transplant patients2025
  4. 4Social determinants of health and outcomes in patients with acute leukemia: Interim results from a prospective, single institution study2025
  5. 5Genomic Knowledge and Mistrust Among Families with Sickle Cell Disease2024