Digital Toolkit for Skin Diseases in LMICs (MIND-the-SKIN)
Primary Purpose
Skin Diseases
Status
Recruiting
Phase
Not Applicable
Locations
Côte D'Ivoire
Study Type
Interventional
Intervention
mHealth app
Sponsored by
About this trial
This is an interventional diagnostic trial for Skin Diseases focused on measuring Skin Diseases, Neglected Diseases, Teledermatology, Telemedicine, Remote Consultation
Eligibility Criteria
Phase 2: Local healthcare providers (i.e., doctors, nurses, or community health workers/volunteers)
Inclusion Criteria:
- 18 years or older
- Working at primary health centers or clinics in Cote d'Ivoire
- Able to read and speak fluent French
- Willing to participate in the pilot study for the 3-month study duration and use a provided tablet with the eSkinHealth app if they were assigned to the intervention group
- Able to consent for oneself
Exclusion Criteria:
- Planning to leave their job at the clinics within the study period
- Difficulty operating mobile devices
Phase 3: Patients with skin diseases
Inclusion Criteria:
- Clinically suspected or diagnosed with skin NTDs (Buruli ulcer, leprosy, and yaws) or have other clinically diagnosed skin conditions
- Diagnosed of concomitantly fewer than three identified skin conditions
- Able to consent for oneself
Exclusion Criteria:
- More than three skin conditions
- Clinically diagnosed skin conditions outside of the target site
Sites / Locations
- Rie YotsuRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
With mHealth app
Without mHealth app
Arm Description
Outcomes
Primary Outcome Measures
Differences in case numbers diagnosed and followed up
Differences in case numbers diagnosed and followed up between the intervention group (with the app) and the control group (without the app) will be measured as the primary outcome of this study.
Secondary Outcome Measures
Effectiveness of the app
We will assess the engagement with the app's platform and willingness to use it. The engagement of local healthcare providers will be measured via data usage, including frequency of visit to the platform and time spent there.
Usability of the app
We will assess the usability of the app at baseline, midpoint (6 weeks), and at the end of the study (12 weeks). The outcome measurement is an average score of SUS. The SUS consists of 10 statements with responses in the form of a five-point Likert scale (e.g., 1: strongly disagree, 5: strongly agree). We will use the French-language version of SUS.
Full Information
NCT ID
NCT05300399
First Posted
March 18, 2022
Last Updated
September 25, 2022
Sponsor
Tulane University
Collaborators
Osaka University, Hope Commission International, Institut Pasteur of Cote d'Ivoire, Institut Raoul Follereau, Centre Suisse de Recherches Scientifiques en Cote d'Ivoire, Trilobite, Ltd.
1. Study Identification
Unique Protocol Identification Number
NCT05300399
Brief Title
Digital Toolkit for Skin Diseases in LMICs
Acronym
MIND-the-SKIN
Official Title
MIND-the-SKIN Project: Multi-functional Innovative Digital Toolkit for the Skin Diseases in LMICs and Beyond
Study Type
Interventional
2. Study Status
Record Verification Date
September 2022
Overall Recruitment Status
Recruiting
Study Start Date
February 14, 2022 (Actual)
Primary Completion Date
May 31, 2023 (Anticipated)
Study Completion Date
May 31, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Tulane University
Collaborators
Osaka University, Hope Commission International, Institut Pasteur of Cote d'Ivoire, Institut Raoul Follereau, Centre Suisse de Recherches Scientifiques en Cote d'Ivoire, Trilobite, Ltd.
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
To evaluate the early detection and effective management of skin diseases using the mHealth app in Cote d'Ivoire, a mixed-methods pilot trial will be conducted in Cote d'Ivoire. The pilot trial will consist of 3 phases: phase 1, development and improvement of the mHealth app; phase 2, pilot trial to evaluate the usability of the mHealth app for local healthcare providers in Cote d'Ivoire; and phase 3, pilot trial to evaluate the effectiveness of case detection and management of skin diseases with the mHealth app in Cote d'Ivoire. The pilot study will be implemented as a 2-arm trial with local healthcare providers and patients with skin diseases over a 3-month follow-up period.
Detailed Description
Background: The prevalence of skin diseases is extremely high in sub-Saharan Africa, among which are skin neglected tropical diseases (skin NTDs) that could lead to life-long disabilities and deformities if not diagnosed and treated early. To achieve early detection and early treatment of these skin diseases, we developed a mobile health application (mHealth app): 'eSkinHealth'.
Objective: To evaluate the early detection and effective management of skin diseases using the mHealth app in Cote d'Ivoire.
Methods: A mixed-methods pilot trial will be conducted in Cote d'Ivoire and will consist of 3 phases: phase 1, development and improvement of the mHealth app; phase 2, pilot trial to evaluate the usability of the mHealth app for local healthcare providers in Cote d'Ivoire; and phase 3, pilot trial to evaluate the effectiveness of case detection and management of skin diseases with the mHealth app in Cote d'Ivoire. The pilot study will be implemented as a 2-arm trial with local healthcare providers and patients with skin diseases over a 3-month follow-up period.
Local healthcare providers (i.e., doctors, nurses, or community health workers/volunteers) must meet all eligibility requirements to enroll in the study. Eligible local healthcare providers are; (1) 18 years or older, (2) working at primary health centers or clinics in Cote d'Ivoire, (3) able to read and speak fluent French, (4) willing to participate in the pilot study for the 3-month study duration and use a provided tablet with the eSkinHealth app if they were assigned in the intervention group, and (5) able to consent for oneself. Ineligible local healthcare providers will be defined as those who (1) are planning to leave the job at the clinics within the study period and (2) have difficulty in operating mobile devices.
Eligible patients will be defined as those are; (1) clinically suspected or diagnosed of skin NTDs (Buruli ulcer, leprosy, lymphatic filariasis, yaws, or other skin NTDs) or have other clinically diagnosed skin conditions, (2) diagnosed of concomitantly fewer than three identified skin conditions, and (3) able to consent for oneself. Ineligible patients have (1) more than three skin conditions and (2) clinically diagnosed skin conditions outside of the target site.
For phase 2, we will use a validated questionnaire, the system usability scale (SUS). The outcome measurement is an average score of SUS. The SUS consists of 10 statements with responses in the form of a five-point Likert scale (e.g., 1: strongly disagree, 5: strongly agree). We will use the French-language version of SUS. We will assess the usability at baseline, midpoint (6 weeks), and at the end of the study (12 weeks).
For phase 3, differences in case numbers diagnosed and followed up between the intervention group (with the app) and the control group (without the app) will be measured as the primary outcome of this study. We will also evaluate the effectiveness of the intervention on secondary outcomes, including engagement with the app's platform and willingness to use it. The engagement of local healthcare providers will be measured via data usage, including the frequency of visits to the platform and time spent there.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Skin Diseases
Keywords
Skin Diseases, Neglected Diseases, Teledermatology, Telemedicine, Remote Consultation
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
1364 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
With mHealth app
Arm Type
Experimental
Arm Title
Without mHealth app
Arm Type
No Intervention
Intervention Type
Device
Intervention Name(s)
mHealth app
Intervention Description
The local healthcare providers will be assigned to an intervention group receiving the mHealth app to be used in their daily practices or a control group.
Primary Outcome Measure Information:
Title
Differences in case numbers diagnosed and followed up
Description
Differences in case numbers diagnosed and followed up between the intervention group (with the app) and the control group (without the app) will be measured as the primary outcome of this study.
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
Effectiveness of the app
Description
We will assess the engagement with the app's platform and willingness to use it. The engagement of local healthcare providers will be measured via data usage, including frequency of visit to the platform and time spent there.
Time Frame
12 weeks
Title
Usability of the app
Description
We will assess the usability of the app at baseline, midpoint (6 weeks), and at the end of the study (12 weeks). The outcome measurement is an average score of SUS. The SUS consists of 10 statements with responses in the form of a five-point Likert scale (e.g., 1: strongly disagree, 5: strongly agree). We will use the French-language version of SUS.
Time Frame
12 weeks
10. Eligibility
Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Phase 2: Local healthcare providers (i.e., doctors, nurses, or community health workers/volunteers)
Inclusion Criteria:
18 years or older
Working at primary health centers or clinics in Cote d'Ivoire
Able to read and speak fluent French
Willing to participate in the pilot study for the 3-month study duration and use a provided tablet with the eSkinHealth app if they were assigned to the intervention group
Able to consent for oneself
Exclusion Criteria:
Planning to leave their job at the clinics within the study period
Difficulty operating mobile devices
Phase 3: Patients with skin diseases
Inclusion Criteria:
Clinically suspected or diagnosed with skin NTDs (Buruli ulcer, leprosy, and yaws) or have other clinically diagnosed skin conditions
Diagnosed of concomitantly fewer than three identified skin conditions
Able to consent for oneself
Exclusion Criteria:
More than three skin conditions
Clinically diagnosed skin conditions outside of the target site
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Rie Yotsu, MD, MIPH, DTM&H, PhD
Phone
+1-(504) 988-5388
Email
ryotsu@tulane.edu
Facility Information:
Facility Name
Rie Yotsu
City
Sinfra
Country
Côte D'Ivoire
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Rie Yotsu, Ph.D
12. IPD Sharing Statement
Citations:
PubMed Identifier
35922062
Citation
Yotsu RR, Itoh S, Yao KA, Kouadio K, Ugai K, Koffi YD, Almamy D, Vagamon B, Blanton RE. The Early Detection and Case Management of Skin Diseases With an mHealth App (eSkinHealth): Protocol for a Mixed Methods Pilot Study in Cote d'Ivoire. JMIR Res Protoc. 2022 Sep 21;11(9):e39867. doi: 10.2196/39867.
Results Reference
derived
Learn more about this trial
Digital Toolkit for Skin Diseases in LMICs
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