NCT05741593

Brief Summary

Cerebrovascular accident is the 2nd leading cause of death and the leading cause of disability in the world. There are brakes and levers of medication adherence in the context of secondary prevention treatment in stroke.

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
30

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Apr 2025

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 14, 2023

Completed
9 days until next milestone

First Posted

Study publicly available on registry

February 23, 2023

Completed
2.1 years until next milestone

Study Start

First participant enrolled

April 1, 2025

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2026

Completed
Last Updated

November 18, 2024

Status Verified

November 1, 2024

Enrollment Period

1 year

First QC Date

February 14, 2023

Last Update Submit

November 14, 2024

Conditions

Keywords

Qualitative studysemi-structured interviewantithromboticstrokemedication adherence

Outcome Measures

Primary Outcomes (1)

  • Analysis of the verbatim from the transcription of the recorded interviews.

    Describing the content of discussions, relating to antithrombotic treatment for secondary prevention, between elderly patients previously treated with antithrombotics and admitted to hospital for an ischemic stroke and a pharmacist

    one year

Secondary Outcomes (4)

  • Analysis of verbatim statements from the transcription of recorded interviews on patients' representations and beliefs regarding antithrombotics

    15 to 60 minutes per patient

  • Analysis of verbatim statements from the transcription of recorded interviews on patients' medication adherence to antithrombotics

    15 to 60 minutes per patient

  • Analysis of verbatim statements from the transcription of recorded interviews on the impact of the occurrence of stroke or recurrence of stroke on medication adherence

    15 to 60 minutes per patient

  • Analysis of verbatim statements from the transcription of recorded interviews on the obstacles and levers to medication adherence

    15 to 60 minutes per patient

Study Arms (1)

Patients having had a stroke

elderly patients previously treated with an antithrombotic and admitted to hospital for an ischemic stroke

Other: Analysis of the verbatim from the transcription of the recorded interviews.

Interventions

recorded semi-structured interviews between the patients and the pharmacist

Patients having had a stroke

Eligibility Criteria

Age65 Years - 100 Years
Sexall
Healthy VolunteersNo
Age GroupsOlder Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients aged 65 and over, hospitalized for an ischemic stroke or a recurrence of ischemic stroke, being already treated with an antithrombotic treatment hospitalized at the Charpennes hospital with a plan to return home

You may qualify if:

  • Patients aged 65 and over
  • Patients hospitalized for an ischemic stroke or a recurrence of ischemic stroke, already being treated with an antithrombotic treatment (antiplatelet agent or anticoagulant ) prior to the stroke
  • Patients living at home and with a plan to return home.
  • Patients who did not object to the study and who gave their consent for the recording of the interview

You may not qualify if:

  • Patients with cognitive disorders or stroke sequelae that do not allow a semi-directive interview to be carried out (at medical discretion).
  • Non-French speaking patients

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

institute of aging - Hôpital des Charpennes

Villeurbanne, 69100, France

RECRUITING

MeSH Terms

Conditions

StrokeMedication Adherence

Condition Hierarchy (Ancestors)

Cerebrovascular DisordersBrain DiseasesCentral Nervous System DiseasesNervous System DiseasesVascular DiseasesCardiovascular DiseasesPatient CompliancePatient Acceptance of Health CareTreatment Adherence and ComplianceHealth BehaviorBehavior

Central Study Contacts

Teddy Novais, PharmD, PhD

CONTACT

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

February 14, 2023

First Posted

February 23, 2023

Study Start

April 1, 2025

Primary Completion

April 1, 2026

Study Completion

April 1, 2026

Last Updated

November 18, 2024

Record last verified: 2024-11

Data Sharing

IPD Sharing
Will not share

Locations