Mobile Devices as Educational Skin History Tools
Status: | Completed |
---|---|
Conditions: | Skin Cancer, Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 3/13/2019 |
Start Date: | April 4, 2017 |
End Date: | December 31, 2018 |
Evaluating the Use of Mobile Devices as Educational Tools Regarding Skin History
Part I of this study surveys patients in the Penn Dermatologic Surgery Clinic to evaluate if
a need exists for increased patient understanding of their skin history and which factors, if
any, related to the patient or their skin history are associated with this need. In part II,
the study aim is to evaluate mobile technology as a way of improving patient understanding of
diagnoses, treatments, and procedures. In this part of the study, eligible patients from part
I will be randomized either to a control group that receives the current standard of care
regarding in-clinic counseling, informational handouts, and access to their medical records,
or to an intervention group that in addition to the current standard of care, is setup with a
mobile app, allowing patients to view a skin history summary report and a reference on their
skin findings and procedures. Patients then complete a survey to establish their baseline
understanding of their clinic visit. Three weeks later the patient is emailed a follow-up
survey to assess their understanding of their in-clinic visit. Differences in understanding
between the two study groups will be assessed by comparing the number of correctly answered
survey items regarding their in-clinic visit, both at baseline (immediately following their
surgery) and three weeks later. Qualitative information regarding satisfaction and areas of
improvement will also be collected via survey. Patients who have an appointment during the
study period at the Penn Dermatologic Surgery clinic for a skin excision will be eligible for
inclusion.
a need exists for increased patient understanding of their skin history and which factors, if
any, related to the patient or their skin history are associated with this need. In part II,
the study aim is to evaluate mobile technology as a way of improving patient understanding of
diagnoses, treatments, and procedures. In this part of the study, eligible patients from part
I will be randomized either to a control group that receives the current standard of care
regarding in-clinic counseling, informational handouts, and access to their medical records,
or to an intervention group that in addition to the current standard of care, is setup with a
mobile app, allowing patients to view a skin history summary report and a reference on their
skin findings and procedures. Patients then complete a survey to establish their baseline
understanding of their clinic visit. Three weeks later the patient is emailed a follow-up
survey to assess their understanding of their in-clinic visit. Differences in understanding
between the two study groups will be assessed by comparing the number of correctly answered
survey items regarding their in-clinic visit, both at baseline (immediately following their
surgery) and three weeks later. Qualitative information regarding satisfaction and areas of
improvement will also be collected via survey. Patients who have an appointment during the
study period at the Penn Dermatologic Surgery clinic for a skin excision will be eligible for
inclusion.
Inclusion Criteria:
- Have an appointment in the Penn Dermatologic Surgery Clinic for removal of a skin area
during the study enrollment period
- Possession of a mobile device running iOS with the study mobile app (intervention)
successfully installed (assistance will be provided by research staff if needed)
Exclusion Criteria:
- Children or adolescents, or if the patient is court-ordered to attend residential
alcohol or other drug treatment facilities and therefore considered prisoners
- Patients will also be excluded if they are incompetent to provide informed consent and
HIPAA authorization.
- If the area being operated on is of the genitals or breasts
- If the area being operated on is of the face, and photos of the area cannot be cropped
or the eyes cannot be covered sufficiently such that photos are non-identifying
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