SurvivorLink: Scalability of an Electronic Personal Health Record
- Conditions
- Childhood Cancer
- Interventions
- Behavioral: SurvivorLink
- Registration Number
- NCT03543852
- Lead Sponsor
- Emory University
- Brief Summary
Previous research suggests that children and adolescents with cancer are at heightened risk of late effects that can occur months or years after cancer treatment, yet little is known about programs that increase their return for follow-up cancer care and late effects surveillance. This study will evaluate the impact of an electronic personal health record and education system, SurvivorLink, for pediatric cancer survivors and their caregivers. The researchers will develop a standardized intervention and training for the SurvivorLink trial, followed by conducting a Hybrid Type 1 effectiveness-implementation, clustered randomized, waitlist control trial to evaluate the impact of SurvivorLink on pediatric cancer patients' one year follow-up visits and completion of screening tests. The study will also assess the impact of SurvivorLink on caregiver's patient activation, survivor's and caregiver's quality of life, and self-efficacy to manage a chronic condition. This study will provide the evidence base about the effects of the system to improve follow-up care for children and adolescents with cancer and best practices for implementation for pediatric cancer centers.
- Detailed Description
Interventions for caregivers and pediatric cancer survivors are needed to improve patient-centered care, minimize late effects and promote overall well-being. The purpose of this research is to assess the impact of the SurvivorLink system on implementation and adherence to cancer care and late effects visits/screening. This research projects proposes to develop a standardized process by which to implement SurvivorLink, a personal electronic health record and education system, designed to promote survivor care, within pediatric cancer clinics. This study will use a Hybrid Type 1 effectiveness-implementation, clustered randomized, waitlist control design to evaluate the impact of SurvivorLink on patient health behavior and quality of life outcomes and understand its delivery among 20 pediatric cancer survivor clinics. The researchers will test the effectiveness of SurvivorLink on 1 year follow-up and completed screenings through a clustered randomized waitlist-control trial: ten clinics will administer the intervention to study participants and the other ten clinics will be a wait-list control group where study participants receive usual care.
The study will evaluate the impact of SurvivorLink on patient survivor care visit attendance and risk-based surveillance tests, caregiver's patient activation, survivor's and caregiver's quality of life and self-efficacy to manage a chronic condition. This study is the first comprehensive, effectiveness-implementation study to evaluate the impact of an electronic personal health record (with care plan) and education system for pediatric cancer survivors and their caregivers.
Recruitment & Eligibility
- Status
- ACTIVE_NOT_RECRUITING
- Sex
- All
- Target Recruitment
- 1800
Not provided
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description SurvivorLink SurvivorLink Participants receiving treatment at a pediatric cancer survivor clinic randomized to this study arm will receive education on how to use SurvivorLink, late effects of treatment, and survivorship care through the system.
- Primary Outcome Measures
Name Time Method Completion of follow-up survivorship visit Month 12 The number of participants completing the follow-up survivorship visit will be determined from medical records and compared between study arms.
Completion of recommended screening tests Month 12 The number of participants completing their risk based cancer care (such as screenings and tests) will be determined from medical records and compared between study arms.
- Secondary Outcome Measures
Name Time Method Change in Patient-Reported Outcome Measurement Information System (PROMIS) score Baseline, Month 3, Month 12 Caregiver quality of life will be assessed with the 10-item Patient-Reported Outcome Measurement Information System (PROMIS), Global Health Short Form. This survey is used to evaluate parents' and caregivers' report of their own physical and mental health quality of life. The scoring system allows each of the individual items to be examined separately to gain information about perceptions of physical, mental, and social health, and general perceptions of health. Respondents rate their level of a variety of aspects of health on a scale of 1 to 5 and rate their level of pain between 0 and 10. Responses to some questions are re-coded so that higher scores reflect better functioning.
Change in Pediatric Quality of Life (PedsQL) Health Care Satisfaction Hematology/Oncology Module score Baseline, Month 12 Satisfaction with oncology care will be assessed with the 25-item Pediatric Quality of Life (PedsQL) Health Care Satisfaction Hematology/Oncology Module. The module will be used to capture parent's general satisfaction, satisfaction with staff communication and interaction style, satisfaction with information amount and timeliness, and satisfaction with the staff's emotional support for both the patient and parent. Responses are given on a 5-point Likert scale where 1 = very dissatisfied and 5 = very satisfied. Total raw scores range from 25 to 125 and higher scores indicate higher satisfaction.
Change in Readiness for Transition Questionnaire (RTQ), Adolescent Behavior score Month 3, Month 12 The survivor's readiness for care transition will be assessed with the Readiness for Transition Questionnaire (RTQ). Adolescent behavior is assessed with 10-items asking participants to rate the level of responsibility that the cancer survivor has for their own care on a scale of 1 (not responsible at all) to 4 (almost always responsible). Total scores for this section range from 10 to 40 with higher scores indicating increased responsibility taken.
Change in Survivor's PROMIS Scale - Global Health Month 3, Month 12 The PROMIS -Global Health scale consists of 10 items assessing general domains of health and functioning. The scoring system allows each of the individual items to be examined separately to gain information about perceptions of physical, mental, and social health, and general perceptions of health. Respondents rate their level of a variety of aspects of health on a scale of 1 to 5 and rate their level of pain between 0 and 10. Responses to some questions are re-coded so that higher scores reflect better functioning.
Change in intention to seek cancer-related follow-up care Baseline, Month 3, Month 12 Participants and caregivers will be asked how likely it is that they (or their child) will go to a cancer follow-up visit in the next year. Possible responses include 1 = not sure, 2 =not likely, 3 = likely or 4 = very likely.
Change in Self-Efficacy for Managing Chronic Disease score Baseline, Month 3, Month 12 The Self-Efficacy for Managing Chronic Disease is a 6-item Scale that measures activities related to daily self care in living with a chronic disease. Respondents rate their level of confidence in performing these activities on a scale of 1=not at all to 10=totally confident. Total scores range from 6 to 60 and higher scores indicate increased feelings of self-efficacy.
Change in Patient Activation Measure (PAM) score Baseline, Month 3, Month 12 The Patient Activation Measure (PAM) is a 10-item survey assessing the patient's or caretaker's knowledge, confidence, and willingness to act concerning their own or their child's health. Respondents indicate how much the agree with health related statements on a scale of 1 (strongly disagree) to 4 (strongly agree). Raw scores range from 10 to 40 and higher scores indicate increased confidence with managing health.
Change in Readiness for Transition Questionnaire (RTQ), Parental Involvement score Month 3, Month 12 The survivor's readiness for care transition will be assessed with the Readiness for Transition Questionnaire (RTQ) for teens. Parental involvement is assessed with 10-items rating the level of involvement by parents for the health care of the cancer survivor on a scale of 1 (not involved at all) to 4 (almost always involved). Total scores for this section range from 10 to 40 with higher scores indicating increased parental involvement.
Trial Locations
- Locations (12)
Children's National Medical Center
🇺🇸Washington, District of Columbia, United States
University of Iowa Stead Family Children's Hospital
🇺🇸Iowa City, Iowa, United States
Upstate Medical University
🇺🇸Syracuse, New York, United States
Penn State Children's Hospital
🇺🇸Hershey, Pennsylvania, United States
Arnold Palmer Hospital for Children
🇺🇸Orlando, Florida, United States
Children's Hospital of Orange County
🇺🇸Orange, California, United States
Banner University Medical Center in Tucson
🇺🇸Tucson, Arizona, United States
Phoenix Children's Hospital
🇺🇸Phoenix, Arizona, United States
University of Chicago Medicine Comer Children's Hospital
🇺🇸Chicago, Illinois, United States
Riley Children's Health
🇺🇸Indianapolis, Indiana, United States
University of Pittsburgh Medical Center (UPMC) Children's Hospital of Pittsburgh
🇺🇸Pittsburgh, Pennsylvania, United States
Washington University St. Louis Children's Hospital
🇺🇸Saint Louis, Missouri, United States