Clinical Trials Directory

Trials / Completed

CompletedNCT02373722

Website Application Based Education and Text Messaging in Improving Skin Wound Care in Patients Undergoing Mohs Surgery

Web App Based Patient Education in Mohs Surgery

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
90 (actual)
Sponsor
Wake Forest University Health Sciences · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This randomized clinical trial studies how well website application (web app) based education and text messaging works in improving skin wound care in patients undergoing Mohs surgery (a surgical procedure used to treat skin cancer). Website application and text messaging based education may help patients stick to wound care instructions before and after surgery, lower anxiety level, and may help monitor their activity.

Detailed description

PRIMARY OBJECTIVES: I. To create a web application which will educate dermatologic surgery patients prior to their operations with educational videos. SECONDARY OBJECTIVES: I. To create and evaluate a web based system to send wound care instructions to patients by text message after their operation. II. Qualitative comments from participants and research staff concerning the feasibility of this approach and the use of Fitbit activity trackers as a means to monitor movement restriction. III. The rate of adverse events. OUTLINE: Patients are randomized to 1 of 4 groups. GROUP I: Patients watch an educational video about Mohs surgery before their surgery, a video about wound care after the surgery and receive text messages about wound care on days 1-5 after the surgery. Patients also receive instructions to reduce movement and use a Fitbit activity tracker. Beginning 48 hours after surgery, patients are instructed to apply petroleum jelly twice daily (BID) to the wound area. GROUP II: Patients watch an educational video about Mohs surgery before their surgery, an educational video about wound care after the surgery and receive instructions to reduce movement and use a Fitbit activity tracker. Beginning 48 hours after surgery, patients apply petroleum jelly BID to the wound area. GROUP III: Patients receive text messages about wound care on days 1-5 after the surgery and receive instructions to reduce movement and use a Fitbit activity tracker. Beginning 48 hours after surgery, patients are also instructed to apply petroleum jelly BID to the wound are. GROUP IV: Patients receive no video or text messages. Patients receive instructions to reduce movement and use a Fitbit activity tracker. Beginning 48 hours after surgery, patients are also instructed to apply petroleum jelly BID to the wound area. After completion of study, patients are followed up at 1 week.

Conditions

Interventions

TypeNameDescription
PROCEDUREMohs SurgeryUndergo Mohs surgery
OTHERInternet-Based InterventionWatch website application based educational video
BEHAVIORALTelephone-Based InterventionReceive text messages
OTHEREducational InterventionWatch website application based educational video
BEHAVIORALExercise InterventionUse Fitbit
OTHERPetrolatum-Mineral Oil-Lanolin-Ceresin OintmentApplied to the wound area
OTHERQuestionnaire AdministrationAncillary studies
OTHERSurvey AdministrationAncillary studies

Timeline

Start date
2015-03-01
Primary completion
2016-03-01
Completion
2016-03-01
First posted
2015-02-27
Last updated
2018-07-03

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02373722. Inclusion in this directory is not an endorsement.