Getting Global Rare Disease Insights Through Technology Study
- Conditions
- Mitochondrial DiseasesFabry DiseaseGaucher DiseasePompe DiseaseMetabolic Disease
- Interventions
- Other: Zamplo Digital Health Platform
- Registration Number
- NCT04758130
- Lead Sponsor
- M.A.G.I.C. Clinic LTD
- Brief Summary
This project is a randomized controlled trial to use a mobile health journal, called Zamplo (formerly known as MyHealthJournal or ZoeInsights), to record patient reported outcomes (PROM) in patients with metabolic disorders.
The objective of the study is to assess the feasibility, acceptability and potential effectiveness of the Zamplo.
The primary hypothesis is as follows:
The Zamplo platform will significantly increase patient activation at 6 months post-baseline, defined as an individual's knowledge, skill, and confidence for managing their health and health care.
The primary outcome is as follows:
Patient activation following the use of Zamplo will serve as the primary outcome of interest and will be measured by the Patient Activation Measure (PAM) 13. The PAM 13 shows the degree of the patient's ability to manage their health with confidence by providing a total patient activation score.
Brief Background:
This project is a randomized controlled trial to use a mobile health journal, called Zamplo, to record patient reported outcomes (PROM) in patients with metabolic disorders.
Zamplo is a software as a service (SaaS) digital platform on both iOS and Android platforms that allows real-time entry of patient symptoms and response to medications. It provides the patients with an interface to see their progress, store questions that they will ask at the next clinic visit, record their health data and use their data to engage in their health outcomes. MAGIC Clinic Ltd., which is the largest clinic in Alberta that manages metabolic disorders such as Fabry disease, Pompe disease, and Gaucher disease, will provide access to Zamplo to patients free-of-charge to evaluate its utility in managing the symptoms of their disease.
Brief Study Design:
The study is a two-armed randomized controlled design with 1:1 allocation to treatment (Zamplo app group) or control (usual care) arms, with assessments at four time points: baseline, 1 month, 3 months (primary outcome), 6 months and 12 months follow-up post-baseline. This is an open-label trial.
The investigators intend to recruit 150 participants in this study, with 75 of them being controls.
Inclusion Criteria:
Adult patients with a diagnosis of metabolic disease Access to a smartphone with data connection Willingness to devote 10-15 mins of time in a day to log medications and notes Able to speak and write English sufficiently to complete questionnaires.
Exclusion Criteria:
Insufficient cognitive function to participate in the study The use of any electronic application requires some competency with the software on a cellphone, downloading the application and entering the data. Some patients who are elderly may not be familiar with this technology and would be excluded.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 150
- Adult patients with a diagnosis of metabolic disease
- Access to a smartphone/computer with data connection
- Willingness to devote 10-15 mins of time in a day to log medications and notes
- Able to speak and write English sufficiently to complete questionnaires
- Insufficient cognitive function to participate in the study
- The use of any electronic application requires some competency with the software on a cellphone, downloading the application and entering the data. Some patients who are elderly may not be familiar with this technology and would be excluded.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description App Group Zamplo Digital Health Platform Patients in this group are provided with a link to download the application and their application usage is tracked by the clinic. Placebo Group Zamplo Digital Health Platform Patients in this group are not provided with the clinic link to the application.
- Primary Outcome Measures
Name Time Method Patient Activation 3 Months post baseline Patient activation following the use of Zamplo will serve as the primary outcome of interest and will be measured by the Patient Activation Measure (PAM) 13. The PAM 13 shows the degree of the patient's ability to manage their health with confidence by providing a total patient activation score. The survey will be completed by participants of the two groups at baseline and follow-up time-points.
- Secondary Outcome Measures
Name Time Method Acceptability 3 Months The acceptability of Zamplo will be assessed by patients and informal caregivers.
Self-Efficacy for Managing Chronic Conditions (PROMIS) 3 Months Manage Medications/Treatment: Self-efficacy is defined as confidence in one's ability to successfully perform specific tasks or behaviors. Self Efficacy for Managing Chronic Conditions assesses confidence in one's ability to successfully perform specific tasks or behaviors related to one's health in a variety of situations. Confidence in managing medication schedules of different complexity.
Patient Satisfaction 3 Months This is a survey question asked during Alberta Health Quality Assessments Q11. "Thinking about all of your personal experiences within the past year with the healthcare services in Alberta that we just reviewed, to what degree are you satisfied or dissatisfied with the services you have received?"
Trial Locations
- Locations (1)
M.A.G.I.C. Clinic LTD
🇨🇦Calgary, Alberta, Canada