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Digital Toolkit for Skin Diseases in LMICs

MIND-the-SKIN Project: Multi-functional Innovative Digital Toolkit for the Skin Diseases in LMICs and Beyond

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05300399
Acronym
MIND-the-SKIN
Enrollment
1364
Registered
2022-03-29
Start date
2022-02-14
Completion date
2023-05-31
Last updated
2022-09-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Skin Diseases

Keywords

Skin Diseases, Neglected Diseases, Teledermatology, Telemedicine, Remote Consultation

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.

Interventions

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.

Sponsors

Osaka University
CollaboratorOTHER
Hope Commission International
CollaboratorUNKNOWN
Institut Pasteur of Cote d'Ivoire
CollaboratorOTHER_GOV
Institut Raoul Follereau
CollaboratorUNKNOWN
Centre Suisse de Recherches Scientifiques en Cote d'Ivoire
CollaboratorOTHER
Trilobite, Ltd.
CollaboratorUNKNOWN
Tulane University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion 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

Design outcomes

Primary

MeasureTime frameDescription
Differences in case numbers diagnosed and followed up12 weeksDifferences 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

MeasureTime frameDescription
Effectiveness of the app12 weeksWe 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 app12 weeksWe 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.

Countries

Côte d’Ivoire

Contacts

Primary ContactRie Yotsu, MD, MIPH, DTM&H, PhD
ryotsu@tulane.edu+1-(504) 988-5388

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 11, 2026