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Kilifi Epilepsy Education Program (KEEP): An intervention to reduce the epilepsy treatment gap

The efficacy of an education intervention for people with epilepsy and their caregivers (KEEP): a controlled randomised study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN35680481
Enrollment
740
Registered
2010-01-11
Start date
2009-08-01
Completion date
Unknown
Last updated
2015-01-13

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

Conditions

Epilepsy Nervous System Diseases Epilepsy

Interventions

Each person with epilepsy is randomised to received the intervention or act as a control. Those that are allocated to the intervention will have a care giver identifier and this person together with t
the education programme includes information on the causes and medical treatment of epilepsy.

Sponsors

University College London (UCL) (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. PWE and their caregivers 2. Both male and female, no age limits 3. Where the person with epilepsy is a child, only caregiver will participate

Exclusion criteria

Exclusion criteria: 1. PWE who refuse informed consent 2. Children whose parents refuse informed consent

Design outcomes

Primary

MeasureTime frame
Adherence of PWE to antiepileptic drugs (AEDs) as measured by drug levels. Plasma phenobarbital or phenytoin concentrations will be measured using an Abbott TDx FLx fluorescence polarisation immunoassay analyser (Abbott Laboratories, Diagnostic Division, Abbott Park, IL, USA). Therapeutic levels of AEDs will be defined as plasma concentrations ranging between 10 - 40 µg/mL, for both phenobarbital and phenytoin. Detectable levels of AEDs will be defined as plasma concentrations of greater than or equal to 1 µg/ml for both phenobarbital and phenytoin. Assessed at one year and four years after study onset.

Secondary

MeasureTime frame
Assessed at one year and four years after study onset: 1. Seizure frequency, measured by a questionnaire 2. Quality of life of PWE, measured by quality of life questionnaire using Likert scale (0 = not at all, 1 = rarely, 2 = sometimes, 3 = most of the time, 4 = always) 3. Knowledge, beliefs and attitudes about epilepsy, measured by the Epilepsy beliefs and attitude questionnaire using Likert Scale (0 = don?t know, 1 = not at all, 2 = believe a little, 3 = totally believe)

Countries

Kenya

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 21, 2026