e-Health Care Method for Patients With Osteogenesis Imperfecta (Tele OI) (NCT06555536) | Clinical Trial Compass
CompletedNot Applicable
e-Health Care Method for Patients With Osteogenesis Imperfecta (Tele OI)
Brazil15 participantsStarted 2022-10-20
Plain-language summary
This work seeks to formalize the association between the use of technology and the effective treatment of patients with Osteogenesis Imperfecta, which has not yet been explored in the literature; and aims to prove functional improvement in patients, using the MIF scale (Functional Independence Measure) and telemedicine care in addition to telephysiotherapy; to reduce the cost of treatment, allowing the patient to be treated without leaving their home and bringing greater effectiveness to the follow-up of these patients.
Who can participate
Age range
3 Years – 60 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Osteogenesis Imperfecta patients
* Patients over 3 years old
* Patients must have a smartphone with the possibility of internet access and the capacity to support the Google Meet program (used in teleconsultations).
Exclusion Criteria:
* Patients under 3 years of age
* Patients without any access to any type of internet
* Patients undergoing treatment with pamindronate
* Patients who, due to their older age (above 60 years), were not familiar with a cell phone device to use our application and follow the therapy remotely
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Change Functional Independence Measure (FIM) in OI patients using e-Health
Timeframe: 1 year
Trial details
NCT IDNCT06555536
SponsorPaulo Humberto Mem Martendal Vallandro Costa