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Behavioural Intervention
Experimental for Bleeding disorder
N/A
Waitlist Available
Led By Stan Kachnowski, PhD, MPA
Research Sponsored by Healthcare Innovation Technology Lab
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 5 years
Awards & highlights
No Placebo-Only Group
Summary
The purpose of this study is to evaluate the utility and user experience of a smart phone app for people with medical conditions, used in conjunction with an ActiGraph wearable device and a connected scale.
Eligible Conditions
- Bleeding disorder
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 5 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 5 years
Treatment Details
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: ExperimentalExperimental Treatment1 Intervention
Multiple device intervention
1. SureSource Engage mobile application
2. ActiGraph Link
3. weight scale
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Who is running the clinical trial?
BayerIndustry Sponsor
2,274 Previous Clinical Trials
25,514,672 Total Patients Enrolled
Healthcare Innovation Technology LabLead Sponsor
4 Previous Clinical Trials
202 Total Patients Enrolled
Stan Kachnowski, PhD, MPAPrincipal InvestigatorHealthcare Innovation Technology Lab
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