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Tele-epic (Telemedicine for Epilepsy Care) (Tele-epic)

Primary Purpose

Epilepsy, Epileptic Encephalopathy, Refractory Epilepsy

Status
Recruiting
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Telemedicine
Sponsored by
Azienda Usl di Bologna
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Epilepsy focused on measuring Telemedicine, Epilepsy, Antiepileptic drugs monitoring

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • adult (age>18 yrs) and pediatric (age<18yrs) outpatients with established diagnosis of epilepsy.

Sites / Locations

  • Azienda USL di Bologna
  • Azienda USL di BolognaRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Telemedicine

Usual care

Arm Description

Baseline: in office clinical assessment of all patients (collection of seizure diary). Followup: scheduled 6-month consultations through a telemedicine device providing remote outcome assessment, counselling and follow-up. If required, on call video consultations available by contacting a provider through telemedicine, 3-hr/week.

Baseline: in office clinical assessment of all patients (collection of seizure diary). Followup: scheduled 6-month in-office consultations with outcome assessment, counselling and follow-up. On-call consultations are possible if needed by the patient, by contacting a clinician through an in-office phone call, 3-hr/week.

Outcomes

Primary Outcome Measures

Seizures control through seizure diary
Non-inferiority in seizures control of follow-up procedures through video consultations with telemedicine devices versus in-office, usual care (UC). Outcomes: non-inferiority of mTM on the primary end-point (seizure control assessed through seizure diary) at 18 month follow- up. Assessment of "seizure control" at the end of 18 month-follow-up. Clinical worsening defined as at least 1: (i) fall of at least 2 positions of the following frequency categories: daily/multiple per day; multiple/week, weekly; multiple/month; monthly; multiple/year; annual; (ii) relapse after SF; (iii) new-onset/relapse of convulsive seizures, tonic/atonic seizures with fall, status epilepticus.

Secondary Outcome Measures

Adherence to treatment
Comparing Adherence to treatment (trough anti epileptic drug monitoring) among telemdicne group and usual care group
ADRs - Adverse Events Profile-AEP
Comparing adverse drugs reactions among telemdicne group and usual care group (Adverse Events Profile-AEP)
Quality of life (QoL)
Comparing quality of life among telemdicne group and usual care group (QoL In Epilepsy-QOLIE- 31,1.0,)
Pediatric quality of life (PedsQL)
Comparing pediatric quality of life among telemdicne group and usual care group (Pediatric QoL Inventory-PedsQL)
Mood-disorders - Beck Depression
Comparing the occurence of mood-disorders (Beck Depression Inventory-BDI-II)
Mood-disorders - State-Trait Anxiety
Comparing the occurence of mood-disorders (State-Trait Anxiety Inventory-STAI Y-1,2)
Mood-disorders - Child Behavior
Comparing the occurence of mood-disorders (Child Behavior CheckList-CBCL for patients aged 6-18 yrs)

Full Information

First Posted
July 6, 2020
Last Updated
February 15, 2022
Sponsor
Azienda Usl di Bologna
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1. Study Identification

Unique Protocol Identification Number
NCT04496310
Brief Title
Tele-epic (Telemedicine for Epilepsy Care)
Acronym
Tele-epic
Official Title
Telemedicine With Mobile Internet Devices for Innovative Care of Patients With Epilepsy
Study Type
Interventional

2. Study Status

Record Verification Date
February 2022
Overall Recruitment Status
Recruiting
Study Start Date
July 9, 2020 (Actual)
Primary Completion Date
July 8, 2023 (Anticipated)
Study Completion Date
July 8, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Azienda Usl di Bologna

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Epilepsy is a chronic condition that requires consistent follow-up aimed at seizure control, surveillance of comorbidities, monitoring of antiepileptic drugs (AED) levels and side effects. Patients may encounter difficulties to be assessed adequately and the disease burden is increased by the need for travelling across the country for medical consultations. Driving restrictions are a further limit to access specialized Centers able to provide an integrated approach focused on patient needs. Telemedicine (TM) offers an invaluable support to patient follow-up, joining the sparse distribution of patients in the country with the prompt availability of a team of experts. The project assesses, through a randomized controlled trial, the non-inferiority of TM in monitoring seizure control compared to usual (face-to-face) care. This approach, coupled with a new self home-sampling method for the measurement of AED levels, will reduce health care costs and simplify patients management.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Epilepsy, Epileptic Encephalopathy, Refractory Epilepsy
Keywords
Telemedicine, Epilepsy, Antiepileptic drugs monitoring

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
600 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Telemedicine
Arm Type
Experimental
Arm Description
Baseline: in office clinical assessment of all patients (collection of seizure diary). Followup: scheduled 6-month consultations through a telemedicine device providing remote outcome assessment, counselling and follow-up. If required, on call video consultations available by contacting a provider through telemedicine, 3-hr/week.
Arm Title
Usual care
Arm Type
No Intervention
Arm Description
Baseline: in office clinical assessment of all patients (collection of seizure diary). Followup: scheduled 6-month in-office consultations with outcome assessment, counselling and follow-up. On-call consultations are possible if needed by the patient, by contacting a clinician through an in-office phone call, 3-hr/week.
Intervention Type
Procedure
Intervention Name(s)
Telemedicine
Intervention Description
Telemedicine versus usual care (face to face visit)
Primary Outcome Measure Information:
Title
Seizures control through seizure diary
Description
Non-inferiority in seizures control of follow-up procedures through video consultations with telemedicine devices versus in-office, usual care (UC). Outcomes: non-inferiority of mTM on the primary end-point (seizure control assessed through seizure diary) at 18 month follow- up. Assessment of "seizure control" at the end of 18 month-follow-up. Clinical worsening defined as at least 1: (i) fall of at least 2 positions of the following frequency categories: daily/multiple per day; multiple/week, weekly; multiple/month; monthly; multiple/year; annual; (ii) relapse after SF; (iii) new-onset/relapse of convulsive seizures, tonic/atonic seizures with fall, status epilepticus.
Time Frame
3 years
Secondary Outcome Measure Information:
Title
Adherence to treatment
Description
Comparing Adherence to treatment (trough anti epileptic drug monitoring) among telemdicne group and usual care group
Time Frame
3 years
Title
ADRs - Adverse Events Profile-AEP
Description
Comparing adverse drugs reactions among telemdicne group and usual care group (Adverse Events Profile-AEP)
Time Frame
3 years
Title
Quality of life (QoL)
Description
Comparing quality of life among telemdicne group and usual care group (QoL In Epilepsy-QOLIE- 31,1.0,)
Time Frame
3 years
Title
Pediatric quality of life (PedsQL)
Description
Comparing pediatric quality of life among telemdicne group and usual care group (Pediatric QoL Inventory-PedsQL)
Time Frame
3 years
Title
Mood-disorders - Beck Depression
Description
Comparing the occurence of mood-disorders (Beck Depression Inventory-BDI-II)
Time Frame
3 years
Title
Mood-disorders - State-Trait Anxiety
Description
Comparing the occurence of mood-disorders (State-Trait Anxiety Inventory-STAI Y-1,2)
Time Frame
3 years
Title
Mood-disorders - Child Behavior
Description
Comparing the occurence of mood-disorders (Child Behavior CheckList-CBCL for patients aged 6-18 yrs)
Time Frame
3 years

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: adult (age>18 yrs) and pediatric (age<18yrs) outpatients with established diagnosis of epilepsy.
Facility Information:
Facility Name
Azienda USL di Bologna
City
Bologna
Country
Italy
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
laura licchetta, MD, PhD
Phone
+39 0514966991
Email
laura.licchetta2@unibo.it
Facility Name
Azienda USL di Bologna
City
Bologna
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
laura licchetta, md, phd
Phone
+390514966991
Email
laura.licchetta2@unibo.it

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
34862297
Citation
Licchetta L, Trivisano M, Baldin E, Mohamed S, Raschi E, Mostacci B, Zenesini C, Contin M, Vigevano F, Bisulli F, Tinuper P, Vignatelli L. TELEmedicine for EPIlepsy Care (TELE-EPIC): protocol of a randomised, open controlled non-inferiority clinical trial. BMJ Open. 2021 Dec 3;11(12):e053980. doi: 10.1136/bmjopen-2021-053980.
Results Reference
derived

Learn more about this trial

Tele-epic (Telemedicine for Epilepsy Care)

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