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A Virtual Intervention to Improve Medication Adherence in Pediatric Cancer: MedSupport

Not Applicable
Completed
Conditions
Medication Adherence
Registration Number
NCT05150028
Lead Sponsor
Roswell Park Cancer Institute
Brief Summary

To develop a cancer center level practice intervention to promote treatment adherence and reduce outcome disparities in pediatric cancer survivors

Detailed Description

To conduct a pilot study to assess the feasibility and acceptability of the Social Determinants of Adherence intervention

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
17
Inclusion Criteria

Parents/caregivers of pediatric patients must meet the following criteria to be eligible:

  • Parents/guardians of child that has been diagnosed with any cancer.
  • Parents/guardians of child with any cancer between age 0 and 18.
  • Parents/guardians of child on home-based oral anti-cancer therapy or supportive care therapy.
  • The clinician for the family agrees to participate in the study.
Exclusion Criteria
  • Participants will be excluded from this study if unwilling or unable to complete the assessment in English

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Retention ratesUp to 8 weeks

Feasibility of intervention as assessed by retention rates

Secondary Outcome Measures
NameTimeMethod
Feasibility of universal SDOA screeningup to 8 weeks

Will be assessed by results of SDOA questionnaire an 8 item questionnaire rated on a 5-point Likert scale (0-I never experienced this ; 5 - I experience this quite a lot)

Provider satisfaction with barrier reportsup to 8 weeks

REDCap analytics will track the rate of opened barrier reports

Trial Locations

Locations (1)

Roswell Park Cancer Institute

🇺🇸

Buffalo, New York, United States

Roswell Park Cancer Institute
🇺🇸Buffalo, New York, United States

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