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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03076645
Other study ID # 203594
Secondary ID
Status Completed
Phase N/A
First received February 2, 2017
Last updated October 11, 2017
Start date October 1, 2016
Est. completion date August 10, 2017

Study information

Verified date October 2017
Source Royal Free Hospital NHS Foundation Trust
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study will measure the engagement of people with epilepsy in a mobile phone based messaging platform as well as understand if there is an impact on their self-management


Description:

The primary purpose of this study is to assess a person with epilepsy's level of usage of a mobile messaging application for peer support. The secondary purpose is to understand what characteristics of their group drive different levels of usage and improvements in self-management.

Participants can participate as much or little as they want for a minimum of six weeks. Participants will complete an initial and a final questionnaire.


Recruitment information / eligibility

Status Completed
Enrollment 202
Est. completion date August 10, 2017
Est. primary completion date August 10, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Age, diagnosis of epilepsy, have access to a smartphone capable of running messaging application

Exclusion Criteria:

- A diagnosis of learning disability/difficulty, significant mental health conditions; those in care, bereaved, or prisoners. Any other vulnerable individuals (individuals unable to protect themselves against significant harm or exploitation)

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Facilitator support and education
Group engaged with facilitator support and education

Locations

Country Name City State
United Kingdom Lewisham & Greenwich NHS Trust Lewisham
United Kingdom Barts and The London NHS Trust London
United Kingdom National Hospital for Neurology and Neurosurgery London
United Kingdom Royal Free Hospital London
United Kingdom Kent Community Health NHS Trust Maidstone

Sponsors (1)

Lead Sponsor Collaborator
Royal Free Hospital NHS Foundation Trust

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Engagement Average participant number of posts over time frame assessed by tracking number of participant entries 6 weeks
Secondary Epilepsy self-management Patient activation measure based on self-reported questionnaire Change in Baseline to 6 weeks
Secondary Epilepsy medication adherence Medication adherence based on self-reported questionnaire Change in Baseline to 6 weeks
Secondary Epilepsy quality of life Quality of life in epilepsy metric based on self-reported questionnaire Change in Baseline to 6 weeks
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