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Secondary Prevention By Structured Semi-Interactive Stroke Prevention Package in INDIA (SPRINT INDIA) Study (SPRINT)

Primary Purpose

Stroke

Status
Unknown status
Phase
Not Applicable
Locations
India
Study Type
Interventional
Intervention
Structured Semi-Interactive Stroke Prevention Package
Sponsored by
Christian Medical College and Hospital, Ludhiana, India
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Stroke focused on measuring Secondary Prevention Package, Education

Eligibility Criteria

18 Years - 99 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Age 18 years and above including both men and women
  2. First-ever Ischemic stroke or intracerebral haemorrhage
  3. Between 2 days-3 months of stroke symptom onset
  4. Computed Tomography /Magnetic Resonance Imaging shows recent stroke (infarct and/or hemorrhage)
  5. Able to read and complete simple tasks suggested in the stroke workbook if having aphasia or is illiterate, a caregiver is available to read for the patients and complete the reading/workbook tasks for the patients.
  6. Able to read and possess a working personal mobile cellular device. In case of patients who is not able to read and/or don't have a personal mobile cellular device or unable to use it, a caregiver is available all times who is able to use mobile cellular devices and read to the patient.
  7. Able to watch health education videos on a video player on cellular device or any other video player available to the patient.
  8. Able to come for follow up visits for at least 1 year
  9. Able to provide signed informed consent.

Exclusion Criteria:

  1. Modified Rankin scale score 0 and 1 at the time of enrollment
  2. Limited internet and/or mobile accessibility due to travel
  3. Patients having active malignancies needing intensive therapy
  4. Patients with a terminal illness with an anticipated lifespan of less than 1 year
  5. Patients with heart failure admitted more than twice in the last six months
  6. Patients with current psychiatric illness with loss of insight and suicide attempts
  7. Patients with cerebral venous sinus thrombosis, aneurysmal subarachnoid haemorrhage, isolated central nervous system vasculitis and systemic vasculitis

Sites / Locations

  • Christian Medical College and HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

No Intervention

Arm Label

Structured Semi-Interactive Prevention

Control group

Arm Description

The intervention arm will receive a Structured Semi-Interactive Stroke Prevention Package including patient workbook, short messaging services and health education videos for a period of one-year in addition to standard of care as per current guidelines

Patients will receive standard post stroke care for 1 year

Outcomes

Primary Outcome Measures

Cardiovascular event
Primary outcome measure is a composite endpoint of Recurrent Stroke, high-risk Transient Ischemic Attack, Acute Coronary Syndrome and Death.

Secondary Outcome Measures

Systolic Blood Pressure (mmHg)
SBP is independent secondary outcome measure. Systolic Blood pressure will be assessed at baseline and one year. Limit 90-250. Lower score, better outcome.
Fasting Blood Glucose (mg/dl)
Fasting Blood Glucose will be assessed at baseline and one year. Limit 90-250. Lower score, better outcome. Limit 30-1000. Lower score, better outcome.
LDL Cholesterol (mg/dl)
LDL Cholesterol will be assessed at baseline and one year. Limit 30-1000. Lower score, better outcome.
Triglycerides (mg/dl)
Triglycerides will be assessed at baseline and one year. Limit 30-1500. Lower score, better outcome.
Smoking cessation (No/ total %)
Smoking cessation will be assessed at baseline and one year. Cessation of smoking at 1 year means better outcome.
Alcohol cessation
Alcohol cessation will be assessed at baseline and one year. Cessation of alcohol at 1 year means better outcome.
Body Mass Index (kg/m2)
Body Mass Index will be assessed at baseline and one year. Limit 15-50. Lower score, better outcome.
Physical Activity MET (min/week)
Physical Activity MET (Metabolic Equivalent of Task) will be assessed at baseline and one year. Limit 0-40000. Higher score better outcome.
Intervention Non-Compliance Assessment (INCA)
Intervention Non-Compliance Assessment (INCA) will be assessed at baseline and one year. This measures is to note the adherence to the medication for the baseline to one year follow-up. The assessment is not score based. the question: "Have you missed your medication ever?", the more the patients mark NO will have the better outcome.
Modified Rankin Scale (mRS)
Modified Rankin Scale will be assessed at baseline and one year. Limit 0-5. Lower score, better outcome.
Diastolic Blood Pressure (mmHg)
Diastolic Blood pressure will be assessed at baseline and one year. Limit 60-140. A lower score, better outcome.

Full Information

First Posted
February 3, 2017
Last Updated
July 26, 2021
Sponsor
Christian Medical College and Hospital, Ludhiana, India
Collaborators
Indian Council of Medical Research
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1. Study Identification

Unique Protocol Identification Number
NCT03228979
Brief Title
Secondary Prevention By Structured Semi-Interactive Stroke Prevention Package in INDIA (SPRINT INDIA) Study
Acronym
SPRINT
Official Title
Secondary Prevention By Structured Semi-Interactive Stroke Prevention Package in INDIA (SPRINT INDIA) Study
Study Type
Interventional

2. Study Status

Record Verification Date
July 2021
Overall Recruitment Status
Unknown status
Study Start Date
April 28, 2018 (Actual)
Primary Completion Date
March 30, 2022 (Anticipated)
Study Completion Date
March 30, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Christian Medical College and Hospital, Ludhiana, India
Collaborators
Indian Council of Medical Research

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
Recurrent stroke, cardiovascular morbidity and mortality are important causes of poor outcome in patients with index stroke. According to the INTERSTROKE study, 80% of stroke are preventable due to the presence of modifiable risk factors. However, the lack of knowledge that stroke and cardiovascular diseases are preventable is a major hurdle to reduce the incidence of recurrent stroke and cardiovascular morbidity. This is further compounded by the non-compliance to medications, exercises smoking cessation and other lifestyle modifications. Stroke awareness has proven to be useful in improving the early arrival of stroke patients to emergency thus increasing the thrombolysis rates. Early stroke prevention education using print and audio-visual media may be useful. In addition, the use of pervasive mobile phone platform may help us reach patients during multiple intervals in a timely manner. The study aims to use structured semi-interactive stroke prevention package to reduce the risk of recurrent strokes, myocardial infarction and death in patients with sub-acute stroke.
Detailed Description
Stroke is the second leading cause of death worldwide in 2010. In rural Maharashtra, it is the leading cause of death. The Stroke incidence in India ranges from 135 to 145 per 100,000 population. From the recent Ludhiana population-based Stroke Registry and also from the INSPIRE Registry 25% of the patients are below 49 years of age. Hypertension, smoking, alcohol, diabetes, heart disease and lifestyle-related problems are the common causes of stroke in India. Rheumatic heart disease and cerebral venous thrombosis are the main etiologies of stroke in the young in our country. Recurrent stroke In an Oxfordshire Community Stroke Project reported in 1994, it was found that actuarial risk of suffering a recurrence was 30% (95% confidence interval, 20% to 39%) by 5 years, about nine times the risk of stroke in the general population. The risk was highest early after the first stroke: 13% (95% confidence interval, 10% to 16%) by 1 year, 15 times the risk in the general population. After the first year, the average annual risk was about 4%. In the Copenhagen Stroke Study, stroke was recurrent in 23% despite most of these patients being given prophylactic treatment prior to recurrence. Only 12% of patients with atrial fibrillation were receiving anticoagulant treatment prior to recurrence. In multivariate analysis, recurrence was more frequently associated with a history of transient ischemic attack (TIA), atrial fibrillation, male gender, and hypertension, but not with age, daily alcohol consumption, smoking, diabetes, ischemic heart disease, serum cholesterol or hematocrit. Mortality was almost doubled compared with patients with a first-ever stroke. In survivors, however, both neurologic and functional outcomes and the speed of recovery were, in general, similar in the two groups. Despite similar neurologic impairments, patients with recurrence contralateral to their first stroke had markedly more severe functional disability after completed rehabilitation than patients with ipsilateral recurrence, implying that the ability to compensate functionally is decreased in patients with contralateral recurrence. However, recently the rates of stroke recurrence have changed in developed countries. On average, the annual risk for future ischemic stroke after an initial ischemic stroke or TIA is ≈3% to 4%. Recent clinical trials of patients with non-cardio embolic ischemic stroke suggest the risk may be as low as 3%, but these data probably underestimate the community-based rate. The estimated risk for an individual patient will be affected by specific characteristics of the event and the person, including age, event type, comorbid illness, and adherence to preventive therapy. The current average annual rate of future stroke (≈3%-4%) represents a historical low that is the result of important discoveries in prevention science. These include antiplatelet therapy and effective strategies for the treatment of hypertension, atrial fibrillation, arterial obstruction and hyperlipidemia. Even in developed nations currently, there are large gaps in the utilization of preventive drugs, control of risk factors, and uptake of lifestyle-changing behaviours. This is often because of failure in the initiation of secondary prevention. Novel methods to improve the risk factor control to prevent recurrent stroke In 2017, the number of mobile phone users is forecast to reach 4.77 billion. The number of mobile phone users in the world is expected to pass the five billion mark by 2019. In 2014, nearly 60 per cent of the population worldwide already owned a mobile phone. Mobile phone text messages can be used to remind, encourage, and motivate patients to adhere to secondary prevention strategies, but there has been limited robust scientific evaluation of these interventions. Recurrent stroke in India Data on recurrent stroke and its causes are scarce from low and middle-income countries like India. In the door-to-door survey done in Kolkata, 15% of patients had a recurrent stroke.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stroke
Keywords
Secondary Prevention Package, Education

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Study is a multicenter, randomized, parallel-design, adaptive and blinded end-point clinical trial of sub-acute stroke patients
Masking
Outcomes Assessor
Masking Description
Blinded end-point clinical trial
Allocation
Randomized
Enrollment
5830 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Structured Semi-Interactive Prevention
Arm Type
Active Comparator
Arm Description
The intervention arm will receive a Structured Semi-Interactive Stroke Prevention Package including patient workbook, short messaging services and health education videos for a period of one-year in addition to standard of care as per current guidelines
Arm Title
Control group
Arm Type
No Intervention
Arm Description
Patients will receive standard post stroke care for 1 year
Intervention Type
Other
Intervention Name(s)
Structured Semi-Interactive Stroke Prevention Package
Intervention Description
The intervention arm will receive a Structured Semi-Interactive Stroke Prevention Package including patient workbook, short messaging services and health education videos for a period of one-year in addition to standard of care as per current guidelines.
Primary Outcome Measure Information:
Title
Cardiovascular event
Description
Primary outcome measure is a composite endpoint of Recurrent Stroke, high-risk Transient Ischemic Attack, Acute Coronary Syndrome and Death.
Time Frame
One year.
Secondary Outcome Measure Information:
Title
Systolic Blood Pressure (mmHg)
Description
SBP is independent secondary outcome measure. Systolic Blood pressure will be assessed at baseline and one year. Limit 90-250. Lower score, better outcome.
Time Frame
One year.
Title
Fasting Blood Glucose (mg/dl)
Description
Fasting Blood Glucose will be assessed at baseline and one year. Limit 90-250. Lower score, better outcome. Limit 30-1000. Lower score, better outcome.
Time Frame
One year.
Title
LDL Cholesterol (mg/dl)
Description
LDL Cholesterol will be assessed at baseline and one year. Limit 30-1000. Lower score, better outcome.
Time Frame
One year.
Title
Triglycerides (mg/dl)
Description
Triglycerides will be assessed at baseline and one year. Limit 30-1500. Lower score, better outcome.
Time Frame
One year.
Title
Smoking cessation (No/ total %)
Description
Smoking cessation will be assessed at baseline and one year. Cessation of smoking at 1 year means better outcome.
Time Frame
One year.
Title
Alcohol cessation
Description
Alcohol cessation will be assessed at baseline and one year. Cessation of alcohol at 1 year means better outcome.
Time Frame
One year.
Title
Body Mass Index (kg/m2)
Description
Body Mass Index will be assessed at baseline and one year. Limit 15-50. Lower score, better outcome.
Time Frame
One year.
Title
Physical Activity MET (min/week)
Description
Physical Activity MET (Metabolic Equivalent of Task) will be assessed at baseline and one year. Limit 0-40000. Higher score better outcome.
Time Frame
One year.
Title
Intervention Non-Compliance Assessment (INCA)
Description
Intervention Non-Compliance Assessment (INCA) will be assessed at baseline and one year. This measures is to note the adherence to the medication for the baseline to one year follow-up. The assessment is not score based. the question: "Have you missed your medication ever?", the more the patients mark NO will have the better outcome.
Time Frame
One year.
Title
Modified Rankin Scale (mRS)
Description
Modified Rankin Scale will be assessed at baseline and one year. Limit 0-5. Lower score, better outcome.
Time Frame
One year.
Title
Diastolic Blood Pressure (mmHg)
Description
Diastolic Blood pressure will be assessed at baseline and one year. Limit 60-140. A lower score, better outcome.
Time Frame
One year.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
99 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 18 years and above including both men and women First-ever Ischemic stroke or intracerebral haemorrhage Between 2 days-3 months of stroke symptom onset Computed Tomography /Magnetic Resonance Imaging shows recent stroke (infarct and/or hemorrhage) Able to read and complete simple tasks suggested in the stroke workbook if having aphasia or is illiterate, a caregiver is available to read for the patients and complete the reading/workbook tasks for the patients. Able to read and possess a working personal mobile cellular device. In case of patients who is not able to read and/or don't have a personal mobile cellular device or unable to use it, a caregiver is available all times who is able to use mobile cellular devices and read to the patient. Able to watch health education videos on a video player on cellular device or any other video player available to the patient. Able to come for follow up visits for at least 1 year Able to provide signed informed consent. Exclusion Criteria: Modified Rankin scale score 0 and 1 at the time of enrollment Limited internet and/or mobile accessibility due to travel Patients having active malignancies needing intensive therapy Patients with a terminal illness with an anticipated lifespan of less than 1 year Patients with heart failure admitted more than twice in the last six months Patients with current psychiatric illness with loss of insight and suicide attempts Patients with cerebral venous sinus thrombosis, aneurysmal subarachnoid haemorrhage, isolated central nervous system vasculitis and systemic vasculitis
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jeyaraj D Pandian, MD DM
Phone
9915784750
Email
jeyarajpandian@hotmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jeyaraj D Pandian, MD DM
Organizational Affiliation
Christian Medical College and Hospital, Ludhiana, India
Official's Role
Principal Investigator
Facility Information:
Facility Name
Christian Medical College and Hospital
City
Ludhiana
State/Province
Punjab
ZIP/Postal Code
141008
Country
India
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jeyaraj D Pandian, MD DM
Phone
9915784750
Email
jeyarajpandian@hotmail.com
First Name & Middle Initial & Last Name & Degree
Jeyaraj D Pandian, MD DM FRACP

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
All information collected from medical records for the study will be stored electronically in a specifically designed database at the Christian Medical College and Hospital, Ludhiana. Participants information will be identified only by their initials, date of birth and a study registration number. Any information transferred electronically will be coded to protect confidentiality. All computer records will be password protected. The study results may be presented at conferences or in scientific publications, but individual participants will not be identifiable. If needed, data will be available in future for other researchers outside the primary research group for secondary purposes, such as meta-analyses, reanalysis, or replication of results.
Citations:
PubMed Identifier
22267690
Citation
Chow CK, Redfern J, Thiagalingam A, Jan S, Whittaker R, Hackett M, Graves N, Mooney J, Hillis GS. Design and rationale of the tobacco, exercise and diet messages (TEXT ME) trial of a text message-based intervention for ongoing prevention of cardiovascular disease in people with coronary disease: a randomised controlled trial protocol. BMJ Open. 2012 Jan 19;2(1):e000606. doi: 10.1136/bmjopen-2011-000606. Print 2012.
Results Reference
background
PubMed Identifier
26486857
Citation
Kamal AK, Shaikh Q, Pasha O, Azam I, Islam M, Memon AA, Rehman H, Akram MA, Affan M, Nazir S, Aziz S, Jan M, Andani A, Muqeet A, Ahmed B, Khoja S. A randomized controlled behavioral intervention trial to improve medication adherence in adult stroke patients with prescription tailored Short Messaging Service (SMS)-SMS4Stroke study. BMC Neurol. 2015 Oct 21;15:212. doi: 10.1186/s12883-015-0471-5.
Results Reference
background
PubMed Identifier
34813082
Citation
Crocker TF, Brown L, Lam N, Wray F, Knapp P, Forster A. Information provision for stroke survivors and their carers. Cochrane Database Syst Rev. 2021 Nov 23;11(11):CD001919. doi: 10.1002/14651858.CD001919.pub4.
Results Reference
derived
PubMed Identifier
31852411
Citation
Kate MP, Arora D, Verma SJ, Sylaja PN, Renjith V, Sharma M, Pandian JD; SPRINT India Collaborators. Secondary Prevention by Structured Semi-Interactive Stroke Prevention Package in India (SPRINT INDIA) study protocol. Int J Stroke. 2020 Jan;15(1):109-115. doi: 10.1177/1747493019895653. Epub 2019 Dec 18.
Results Reference
derived

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Secondary Prevention By Structured Semi-Interactive Stroke Prevention Package in INDIA (SPRINT INDIA) Study

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