New program aims to cut seizures and boost quality of life for epilepsy patients in uganda
NCT ID NCT06139198
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests a 12-week self-management program (SMART-U) for adults with epilepsy in Uganda. The program includes group sessions and phone follow-up to help people manage their condition. Researchers will compare seizure frequency and quality of life between those in the program and those receiving usual care, with 190 participants total.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Self-management behavioral program (SMART-U)
- What this could lead to
- If successful, this program could provide a low-cost way for people with epilepsy in Uganda to better control seizures and improve their daily lives.
- What could go wrong
- This is a relatively small, early-stage trial focused on behavioral change, not a new drug. Results may not apply to other settings, and the program requires significant time commitment from participants.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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190 people
The number who actually took part.
- Started
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Jan 2025
- Expected to finish
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Jul 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Participants will have a clinical diagnosis of epilepsy documented with at least two outpatients visits; this will ensure that the study participants have been taking ASMs but still getting breakthrough seizures. 2. ≥ age 18, attending the neurology clinics, 3. Be able to provide written informed consent by the study participant or immediate caregiver/legal guardian, 4. Ability to participate in study procedures, this is due to time required to attend and participate in the scheduled sessions which may last between 45mins - 1 hour. 5. and have had at least 1 seizure in the past 6 months. 6. Owning a mobile phone either by the PWE or immediate caregiver Exclusion Criteria: 1. Participants with dementia 2. Participants who are pregnant (given the likely need of different and more intensive treatments among pregnant PWE that may affect their ability to participate in the SMART-U sessions regularly. 3. Or those who are unable to participate in study procedures.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Mulago National Referral and Teaching Hospital
Kampala, Uganda
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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