Pilot Study of the Pragmatic Use of Mobile Phone Based Follow up of Actinic Keratoses Treated With Topical 5-fluorouracil

Sponsor
University of California, Davis (Other)
Overall Status
Completed
CT.gov ID
NCT02938715
Collaborator
(none)
26
1
2
11
2.4

Study Details

Study Description

Brief Summary

In this study, subjects who are attending the dermatology clinic and who have already been prescribed topical 5-fluorouracial for the treatment of actinic keratoses as part of their standard of care will be recruited. The purpose of the study is to assess patient satisfaction when engaging in follow up treatment of actinic keratosis via the HIPAA-compliant teledermatology platform called Klara. Additionally, the goal is to assess the difference in total duration of treatment between treatment and control group. A total of 50 subjects will be enrolled and will be randomly assigned into the treatment group (teledermatology group; n=25) or control group (telephone only group; n=25).

Condition or Disease Intervention/Treatment Phase
  • Other: teledermatology feedback
N/A

Detailed Description

Objectives

To assess patient satisfaction when engaging in follow up treatment of actinic keratoses:

Follow up of subjects with actinic keratoses (AK) who have been prescribed topical 5-fluorouracil (5-FU) therapy as part of their standard of care.

To assess the difference in total dose of exposure to 5-FU between treatment and control group.

Background

Teledermatology is a growing field within dermatology that has started to adapt the use of mobile phone technology (1). The growth of teledermatology has allowed greater access to care in both the inpatient and outpatient setting (1, 2), as well as in educational services (3). The aim of this study is to investigate how mobile phone photographic teledermatology can be adapted for use in the dermatology clinic to continually engage with the patient. More specifically, the researchers seek to understand how mobile phone technology can be used in the evaluation of subjects on topical 5-FU therapy for their actinic keratoses.

Diffuse actinic damage is typically treated with field therapy (4) that involves the use of topical 5-FU. Patients are advised to apply the cream twice daily for 2-4 weeks (5). However, many patients note misunderstanding with these instructions (6). Typical follow up has included telephone based grading and in person follow up (5). However, a return visit to the clinic can be both burdensome to the patient and fill up the clinic with follow up appointments instead of allowing the appointment slot to go to examination of a new patient, thereby reducing access to care for other patients. Telephone conversations are not based on a physical exam and thus do not allow for objective evaluation of the treatment area. For this reason, the researchers seek to use mobile phone photography to evaluate patients with actinic keratoses on topical 5-FU treatment.

Study Design

Study Type:
Interventional
Actual Enrollment :
26 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Pilot Study of the Pragmatic Use of Mobile Phone Based Follow up of Actinic Keratoses Treated With Topical 5-fluorouracil
Actual Study Start Date :
Oct 1, 2016
Actual Primary Completion Date :
Sep 1, 2017
Actual Study Completion Date :
Sep 1, 2017

Arms and Interventions

Arm Intervention/Treatment
Experimental: Feedback group (teledermatology)

Other: teledermatology feedback
subject provided feedback to continue or discontinue their cream (based on actinic keratoses grading and lesion counting)

No Intervention: Control group (phone only)

Outcome Measures

Primary Outcome Measures

  1. Difference in total dose of exposure to 5-FU between teledermatology and control group (measured as days of exposure x frequency of application per day) [4 weeks]

    The total exposure to 5-FU will be calculated as total doses over 4 week period.

Secondary Outcome Measures

  1. Patient satisfaction assessment [4 weeks and 8 weeks]

  2. Change in clinical grading of actinic keratoses [baseline and weeks 1, 2, 3, 4, 8]

  3. Change in AK lesion count [baseline and weeks 1, 2, 3, 4, 8]

  4. Change in severity of symptoms [baseline and weeks 1, 2, 3, 4, 8]

  5. Difference in adverse effects including erythema, pruritus, burning, soreness, and/or tenderness, crusting and/or erosions, scaling and/or flaking, and swelling [baseline and weeks 1, 2, 3, 4, 8]

  6. Difference in number of clinic visits between the 2 groups [8 weeks]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Subjects 18 years of age or older

  • Subjects who have already been prescribed topical 5-fluorouracil for treatment of scalp, facial, arm, or hand actinic keratoses but have not initiated treatment yet

Exclusion Criteria:
  • Adults unable to consent

  • Non English speaking or illiterate

  • Subjects with known allergy to 5-fluorouracil

  • Subjects who do not have access to a smartphone capable of engaging with the online teledermatology platform

  • Pregnant women

  • Prisoners

Contacts and Locations

Locations

Site City State Country Postal Code
1 UC Davis Department of Dermatology Sacramento California United States 95816

Sponsors and Collaborators

  • University of California, Davis

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
University of California, Davis
ClinicalTrials.gov Identifier:
NCT02938715
Other Study ID Numbers:
  • 955458
First Posted:
Oct 19, 2016
Last Update Posted:
Jan 16, 2018
Last Verified:
Jan 1, 2018
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 16, 2018