Using Information Technology to Improve Outcomes for Children Living With Cancer
- Conditions
- Cancer
- Interventions
- Behavioral: Symptom Monitoring & Systematic Assessment and Reporting System in Young Survivors (SyMon-SAYS)
- Registration Number
- NCT04789720
- Lead Sponsor
- Northwestern University
- Brief Summary
This proposed study plans to develop and evaluate a patient-oriented, technology-based, symptom monitoring system that reports symptoms experienced by children with cancer to their parents and health care providers.
- Detailed Description
Cancer is a leading cause of death and disability in children under 15 years of age. Its unrelieved symptoms and side effects of often-aggressive treatments can lead to poor psychosocial functioning and decreased health-related quality of life (HRQOL) for patients and their families. Barriers at the patient, healthcare provider and system levels can contribute to poor symptom management. A technology-based program can minimize these barriers by routinely collecting and interpreting patient-reported outcomes (PROs) and patient/parent contextual data in pediatric oncology ambulatory settings in a manner that is efficient, actionable by physicians, supports engagement of patients and families with their health and care, and improves clinical processes and outcomes. This proposed project will develop and evaluate the effectiveness of such a program: Symptom Monitoring \& Systematic Assessment and Reporting System in Young Survivors (SyMon-SAYS). We hypothesize that the SyMon-SAYS intervention will decrease parent-perceived barriers to managing their child's symptoms, decrease patient symptom burden, increase patients' and parents' self-efficacy, and ultimately increase patient HRQOL.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 200
Patients
- Have an hematology/oncologic diagnosis (including a brain tumor)
- Be on-treatment or within 6 months post-therapy
- Be between 8 and 17 years old
- English-speaking
- Have sufficient cognitive and motor abilities to complete survey via an electronic device (e.g., smartphone, iPAD, etc.) or computer
- Be able and willing to sign assent forms (for those 12-17 years old).
Parent/legal guardian
- Be a parent (father or mother) or a legal guardian of eligible patients
- Demonstrates sufficient English and/or Spanish ability to understand and sign the informed consent form
- Have sufficient cognitive and motor abilities to complete survey via an electronic device (e.g., smartphone, iPAD, etc) or computer
- Patients who cannot understand English sufficiently to sign consent/assent form
- Patients who cannot understand English sufficiently to complete the questionnaires
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description SyMon-SAYS Waitlist Control (Group B) Symptom Monitoring & Systematic Assessment and Reporting System in Young Survivors (SyMon-SAYS) The waitlist control group participants (Group B) will receive their usual care during weeks 1-8 and will receive the SyMon-SAYS intervention every week during weeks 9-16. SyMon-SAYS Intervention (Group A) Symptom Monitoring & Systematic Assessment and Reporting System in Young Survivors (SyMon-SAYS) Group A participants will receive the SyMon-SAYS intervention every week for 16 weeks.
- Primary Outcome Measures
Name Time Method Adherence to intervention 16 weeks for Group A and 8 weeks for Group B The adherence to the SyMon-SAYS Intervention will be evaluated by using the percentage of dyads completing the symptom assessments at all time-points (16 weeks for Group A participants and 8 weeks for Group B participants), excluding those who are off-study or deceased.
Overall symptom burden change from baseline to week 8; and from week 9 to week 16 Evidence of decreased or maintained symptom burden as measured by the SyMon-SAYS symptom checklist from baseline to week 8 (primary analysis) and from week 9 to week 16. Each symptom is rated by using a 5-point rating scale and will be evaluated separately. Higher scores represent worse symptom burden.
Perceived symptom management barriers as reported by parents of patients change from baseline to week 8; and from week 9 to week 16 Evidence of decreased or maintained perceived symptom barriers as measured by a modified 23-item Symptom Management Barriers Questionnaire checklist from baseline to week 8 (primary analysis) and from week 9 to week 19. Possible scores range from 23 - 115. Higher scores represent more perceived barriers.
Self-Efficacy change from baseline to week 8; and from week 9 to week 16 Evidence of improved or maintained self-efficacy in managing symptoms related to cancer therapy as measured by using the NIH Toolbox Self-Efficacy (child self-reported version) from baseline to week 8 and from week 9 to week 16. Scores will be reported by using a T-score metric, with a general population mean=50 and SD=10. Higher scores represent better self-efficacy.
Health related quality of life change from baseline to week 8; and from week 9 to week 16 Evidence of improved or maintained health related quality of life (physical function, fatigue, depressive symptom, anxiety, anger, social functioning), as measured by the pediatric Patient Reported Outcome Measurement Information System, PROMIS, (child self-report version) from baseline to week 8 as well as from week 9 to week 16. Scores will be reported by using a T-score system, in which mean of the norming group =50 and SD=10. Higher scores represent better functioning (mobility, upper extremity function, peer relationships) or worse symptoms (depression, anxiety, anger and fatigue).
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Ann & Robert H. Lurie Childrens Hospital of Chicago
🇺🇸Chicago, Illinois, United States