An observational study in Skin Conditions and Traditional Medicine, sponsored by University of Edinburgh. Not yet recruiting. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-09-28.
Sponsored by University of Edinburgh · Observational
This study aims to understand how people in Blantyre, Malawi recognise and manage common skin problems, and what role traditional medicine plays in their care. The main question it aims to answer are:
This is an 8-week study through which is intended to conduct a review of the use of traditional medicine in dermatologic care through interviews with patients and traditional healers. The findings would allow equitable knowledge exchange about presentations of skin conditions on black skin and treatment approaches that center African knowledge systems.
Within Western medical education, in lectures and medical textbooks, there is a lack of teaching and images depicting the presentation of skin conditions on darker skin. This is a problem because diagnosis is dependent on the pattern recognition skills of the clinician, therefore, a lack of exposure to images of darker skin increases the chance of misdiagnosis. In various countries in sub-Saharan Africa, there are few dermatologists in the region and healthcare workers in the primary sector are not sufficiently trained to manage common skin conditions. The knowledge generated in Western countries informs practices in sub-Saharan Africa with little adaptation to suit the local needs of the population. This also holds true for the medical training in these countries, which upholds medical racism because the curricula are not decolonised. Apart from the direct practice of dermatology, healthcare workers are also responsible for improving the health literacy of their population. The chief investigator spoke to a doctor currently practising in Malawi, who mentioned that black skin is mostly depicted in books focusing on tropical medicine, while other medical books depict white skin. The intention of this study is to conduct interviews exploring this topic and create drawings that depict skin conditions on darker skin.
It is important to understand the approaches that local cultures use to manage common skin conditions, which range from recognition to treatment strategies. This includes the use of traditional medicine - ethnobotanical practices and healers - that are more easily accessible than the local dermatologists, whose access tends to be limited to the private sector. This study will have a particular focus on how laypeople/the public engage with dermatology.
There is a need for the development of programs and resources that incorporate Western biomedical knowledge with local indigenous ways of knowing. This research is important to bring visibility, as a lack of prioritisation of black skin health in Western countries directly translates to the experience of people dealing with skin conditions in African countries.
496 studies on the registry are indexed under Skin Diseases; 77 are open to participants now.
This study's planned enrollment of 13 is below the median of 165 across 101 observational studies indexed under Skin Diseases.
Browse Skin Diseases studies →University of Edinburgh is the lead sponsor of 403 studies on the registry; 64 are open to participants now.
Counted across the registry records on this site, refreshed daily.
The criteria were revised on the registry on Sep 28, 2026. See what changed
Adults who are clinicians or subject matter experts on skin conditions in Blantyre, Malawi.
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Exclusion criteria
Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Informed consent
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Number and content of themes describing participants' understanding and the role of traditional medicine use in the identification, treatment, and management of skin conditions, using reflexive thematic analysis of the semi-structured interviews
Time frame: Single interview at enrollment
No study locations are listed for this record.
Plan to share: No — This is sensitive information that, if shared, could increase the likelihood of identifying the participants.
Start is estimated for Dec 2026; primary completion for Aug 2027, 8 months later.
How these figures are worked out, and which studies are left out of them.
From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗
This study is not yet recruiting, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.
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