- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03188224
Apply the (MyTransition) App In Transition (ApplyIT)
September 25, 2019 updated by: McMaster University
An App-based Transition Toolkit Targeting Youth With Chronic Health Conditions: A Randomized Trial as a Foundation to Improve Healthcare Transition and Outcomes
Moving from child care to adult care is a hard time for patients and their families.
Parents of children with chronic conditions say they need more support around the time of changing care.
Care providers say they do not have the tools to provide smooth transitions or help their patients manage their own health.
This study is to see if a smart-phone-based app (named MyTransition) can improve healthcare transition experiences and health outcomes for youth, compared to usual care.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Transition to adult care is an unavoidable and challenging period for patients and their families, and comes with adverse outcomes in experience of care, population health, and costs.
Parents of children with chronic conditions report a greater need for support around the time of healthcare transition.
Providers report neither having the tools nor appropriate resources to foster smooth transitions for patients and their families.
We hypothesize that an app-based transition toolkit (named MyTransition) designed to support youth moving from child to adult care can improve their experiences and lead to better health.
The main objective of this study is to collect information to design a large multi-centre randomized control trial to assess implementation of the MyTransition app including recruitment, completion of follow-up, and scale-ability of the intervention.
The secondary objective is to assess the feasibility and potential effect of the MyTransition app-based transition toolkit for improving health of youth (quality of life), healthcare transition experience, and achievement of health and life goals.
Study Type
Interventional
Enrollment (Actual)
39
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Ontario
-
Hamilton, Ontario, Canada, L8N 3Z5
- McMaster Children's Hospital
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
14 years to 18 years (Child, Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Attending participating clinic at McMaster Children's Hospital
- Diagnosed with chronic health condition
- Must be able to utilize the intervention tool
- Must be able to read and understand English
Exclusion Criteria:
- Dependence on caregivers in areas of daily functioning, self-care and/or communication
- Inability to lead or provide own care
- Enrolled in a potentially confounding trial
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Control
Usual care
|
|
|
Experimental: Intervention
MyTransition app
|
MyTransition app is designed to support youth moving from pediatric to adult healthcare.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Completion of Data Collection
Time Frame: 6-Month Follow-Up
|
Completion rate of 90% for all outcomes.
|
6-Month Follow-Up
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Short Form Six-Dimension (SF-6D)
Time Frame: Baseline, 3-month follow-up, 6-month follow-up
|
Instrument for describing and valuing individual's health.
Will be used to evaluate quality of life.
|
Baseline, 3-month follow-up, 6-month follow-up
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Client Satisfaction Questionnaire (CSQ-8)
Time Frame: Baseline, 3-month follow-up, 6-month follow-up
|
Designed to measure satisfaction with health and human services received by individuals and families.
Will be used to assess healthcare transition experience.
|
Baseline, 3-month follow-up, 6-month follow-up
|
|
Change in Transition-Q
Time Frame: Baseline, 3-month follow-up, 6-month follow-up
|
Measures transition readiness/self-management ability.
Will be used to evaluate readiness for transition.
|
Baseline, 3-month follow-up, 6-month follow-up
|
|
Change in Transition Readiness Assessment Questionnaire (TRAQ)
Time Frame: Baseline, 3-month follow-up, 6-month follow-up
|
Patient-centered questionnaire that providers and families use to assess youths' ability to make appointments, to understand their medications, and to develop other skills needed for transition to adult care.
Will be used to evaluate readiness for transition.
|
Baseline, 3-month follow-up, 6-month follow-up
|
|
Change in Canadian Occupational Performance Measure (COPM)
Time Frame: Baseline, 3-month follow-up, 6-month follow-up
|
Designed to measure satisfaction with health and human services received by individuals and families.
Will be used to determine achievement of health and life goals.
|
Baseline, 3-month follow-up, 6-month follow-up
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Jan Willem Gorter, PhD, McMaster University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 25, 2018
Primary Completion (Actual)
December 20, 2018
Study Completion (Actual)
December 20, 2018
Study Registration Dates
First Submitted
June 13, 2017
First Submitted That Met QC Criteria
June 14, 2017
First Posted (Actual)
June 15, 2017
Study Record Updates
Last Update Posted (Actual)
September 26, 2019
Last Update Submitted That Met QC Criteria
September 25, 2019
Last Verified
September 1, 2019
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- ApplyIT Study
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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