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Telemedicine Efficacy in Medication Adherence in Post-ischemic Stroke Patients

Primary Purpose

Stroke, Compliance, Patient, Compliance, Treatment

Status
Unknown status
Phase
Not Applicable
Locations
Colombia
Study Type
Interventional
Intervention
telemedicine neurology consultation
in-person neurology consultation
Sponsored by
Fundación Cardiovascular de Colombia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Stroke focused on measuring Stroke consultation, Telemedicine, Recovery, Rehabilitation

Eligibility Criteria

18 Years - 86 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • First ischemic stroke.
  • Lived in urban areas.
  • Available Access to permanent internet at home, in work on mobile dispositive, computers or tablets.
  • Patients who gave their written informed consent.

Exclusion Criteria:

  • Diagnosis of neurodegenerative diseases such as dementia and Parkinson's disease.
  • Diagnosis of Diseases-terminal to prevent tracking.
  • Diagnosis of psychiatric illnesses such as major depressive disorder (MDD) or others.
  • Global cognitive impairment or previous diagnosis of dementia.

Sites / Locations

  • Hospital Internacional de ColombiaRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

telemedicine neurology consultation

in-person neurology consultation

Arm Description

Starting on day 12-14 post-discharge, participants will receive a phone call for a drug conciliation. Participants at 1-month post-discharge will receive a telemedicine consultation, another at 3 months and 6 months.

Starting at 1-month post-discharge, participants will attend an in-person neurology consultation and the following consultations depend on their physician's criteria until completed 6 months post-discharge.

Outcomes

Primary Outcome Measures

Percentage medication adherence through Morisky-Green questionnaire
The Morisky Medication Adherence Scale in the original version (MMAS-4) is a structured self-report measure of medication-taking behavior. It consists of 4 items, with binary scoring (yes/no). Patients score one point for every 'Yes' answer. A score of 0 indicates high adherence; a score of 1 or 2 indicates intermediate adherence, and a score of 3 or 4 indicates low adherence.

Secondary Outcome Measures

The Fantastic lifestyle assessment questionnaire
The fantastic instrument consists of a questionnaire with 25 closed-end questions across nine domains of the physical, psychological, and social components of lifestyle. The 23 first questions have multiple-choice (five answers) and the last two are dichotomous. The sum of all points yields a total score that classifies individuals in five categories, as follows: "Excellent" (85 to 100 points), "Very good" (70 to 84 points), "Good" (55 to 69 points), "Regular" (35 to 54 points), and "Needing improvement" (0 to 34 points).
Caregiver burden questionnaire
The Zarit Burden instrument contains 22 items. Each item on the interview is a statement which the caregiver is asked to endorse using a 5-point scale. Response options range from 0 (Never) to 4 (Nearly Always) with the sum of scores ranging between 0-88. Higher scores are taken to indicate increased burden intensity (score: ≤21=no burden; 21-40 = mild burden; 41-60 = moderate burden; ≥61 = severe burden).

Full Information

First Posted
April 26, 2021
Last Updated
August 26, 2021
Sponsor
Fundación Cardiovascular de Colombia
Collaborators
Instituto Colombiano para el Desarrollo de la Ciencia y la Tecnología (COLCIENCIAS)
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1. Study Identification

Unique Protocol Identification Number
NCT04877171
Brief Title
Telemedicine Efficacy in Medication Adherence in Post-ischemic Stroke Patients
Official Title
Telemedicine Efficacy in Medication Adherence in Post-ischemic Stroke Patients
Study Type
Interventional

2. Study Status

Record Verification Date
August 2021
Overall Recruitment Status
Unknown status
Study Start Date
July 16, 2021 (Actual)
Primary Completion Date
July 31, 2022 (Anticipated)
Study Completion Date
August 30, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Fundación Cardiovascular de Colombia
Collaborators
Instituto Colombiano para el Desarrollo de la Ciencia y la Tecnología (COLCIENCIAS)

4. Oversight

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

5. Study Description

Brief Summary
Telemedicine is an incipient resource to support the stroke system of care in Colombia. Several studies had demonstrated that patients benefit by implementing telestroke, for instance, providing timely and appropriate neurological consultation, diminishing accessible barriers, improving medication adherence for secondary prevention and facilitating linkages between patient and physician, especially for those in rural or neurologically underserved areas. Hypothesis: The use of Telemedicine improves medication adherence in Post-ischemic Stroke. Study Design: This is a randomized, single-blind, clinical trial to assess the efficacy of Telemedicine, over medication adherence in Post-ischemic Stroke subjects from Colombia. Population: Eighty-four Post-ischemic Stroke subjects, subjects of both genders, over 18 years old, with a first stroke will be included. Ethical Aspects: The study will be conducted according to the Helsinki declaration, the good clinical practices guidelines and the Colombian legislation. Prior to entering the study, patients must sign a written or oral informed consent that has been approved by the Institutional Ethics Committee of Fundación Cardiovascular de Colombia. Overall objective: this study aims to determine the efficacy of telemedicine on pharmacological adherence in post-ischemic Stroke Participants. Focus of study: Adherence to secondary stroke prevention medication.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stroke, Compliance, Patient, Compliance, Treatment, Compliance, Medication
Keywords
Stroke consultation, Telemedicine, Recovery, Rehabilitation

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
84 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
telemedicine neurology consultation
Arm Type
Experimental
Arm Description
Starting on day 12-14 post-discharge, participants will receive a phone call for a drug conciliation. Participants at 1-month post-discharge will receive a telemedicine consultation, another at 3 months and 6 months.
Arm Title
in-person neurology consultation
Arm Type
Active Comparator
Arm Description
Starting at 1-month post-discharge, participants will attend an in-person neurology consultation and the following consultations depend on their physician's criteria until completed 6 months post-discharge.
Intervention Type
Other
Intervention Name(s)
telemedicine neurology consultation
Intervention Description
consultations via phone-only at 12-14-day post-discharge. Consultations via phone both audio and video at 1, 3 and 6 months
Intervention Type
Other
Intervention Name(s)
in-person neurology consultation
Intervention Description
consultation in-person at Hospital Internacional de Colombia
Primary Outcome Measure Information:
Title
Percentage medication adherence through Morisky-Green questionnaire
Description
The Morisky Medication Adherence Scale in the original version (MMAS-4) is a structured self-report measure of medication-taking behavior. It consists of 4 items, with binary scoring (yes/no). Patients score one point for every 'Yes' answer. A score of 0 indicates high adherence; a score of 1 or 2 indicates intermediate adherence, and a score of 3 or 4 indicates low adherence.
Time Frame
6 months
Secondary Outcome Measure Information:
Title
The Fantastic lifestyle assessment questionnaire
Description
The fantastic instrument consists of a questionnaire with 25 closed-end questions across nine domains of the physical, psychological, and social components of lifestyle. The 23 first questions have multiple-choice (five answers) and the last two are dichotomous. The sum of all points yields a total score that classifies individuals in five categories, as follows: "Excellent" (85 to 100 points), "Very good" (70 to 84 points), "Good" (55 to 69 points), "Regular" (35 to 54 points), and "Needing improvement" (0 to 34 points).
Time Frame
6 months
Title
Caregiver burden questionnaire
Description
The Zarit Burden instrument contains 22 items. Each item on the interview is a statement which the caregiver is asked to endorse using a 5-point scale. Response options range from 0 (Never) to 4 (Nearly Always) with the sum of scores ranging between 0-88. Higher scores are taken to indicate increased burden intensity (score: ≤21=no burden; 21-40 = mild burden; 41-60 = moderate burden; ≥61 = severe burden).
Time Frame
6 months
Other Pre-specified Outcome Measures:
Title
Presence of adverse events related to secondary stroke prevention medication
Description
Thirty days after beginning the treatment, and every consultation month thereafter, the participants will be asked about the occurrence of adverse events.
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
86 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: First ischemic stroke. Lived in urban areas. Available Access to permanent internet at home, in work on mobile dispositive, computers or tablets. Patients who gave their written informed consent. Exclusion Criteria: Diagnosis of neurodegenerative diseases such as dementia and Parkinson's disease. Diagnosis of Diseases-terminal to prevent tracking. Diagnosis of psychiatric illnesses such as major depressive disorder (MDD) or others. Global cognitive impairment or previous diagnosis of dementia.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Federico A Silva, MD, MSc, MBA
Phone
3174358166
Email
federicosilva@fcv.org
Facility Information:
Facility Name
Hospital Internacional de Colombia
City
Piedecuesta
State/Province
Santander,
Country
Colombia
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Federico A Silva, MD, MSc, MBA
First Name & Middle Initial & Last Name & Degree
Jenny P Garzon, MD

12. IPD Sharing Statement

Plan to Share IPD
No
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Telemedicine Efficacy in Medication Adherence in Post-ischemic Stroke Patients

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