- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07351422
Investigating Management, Perspectives and Attitudes Towards Care in Takayasu Arteritis (TAK-IMPACT)
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This study aims to investigate the experiences and perceptions of patients with Takayasu arteritis regarding their disease, as well as the perspectives of physicians regarding the management and treatment of these patients.
Patients with TAK will be invited to complete an anonymous online (Online Surveys) questionnaire, which will take approximately 25 minutes and will consist of multiple-choice and short-answer questions. The questionnaire will ask about their experience with the condition, symptoms, treatments they have received, and any concerns or priorities they have regarding their care.
Physicians who treat TAK will also be invited to complete a separate online questionnaire, taking around 15 minutes and also consisting of multiple-choice and short-answer questions. This will explore how they diagnose and manage TAK, their choice of treatments, and any challenges they face in treating the condition
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Alexandra Armstrong
- Phone Number: +447445695898
- Email: A.Armstrong-9@sms.ed.ac.uk
Study Locations
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-
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Edinburgh, United Kingdom
- Recruiting
- University of Edinburgh
-
Contact:
- Alexandra Armstrong
- Phone Number: +44 7445695898
- Email: A.Armstrong-9@sms.ed.ac.uk
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
For the patient questionnaire:
- Age ≥ 18 years
- A formal diagnosis of TAK
For the physician questionnaire
• A physician involved in the management/decision-making for patients diagnosed with TAK
Exclusion Criteria:
For the patient questionnaire:
- Age < 18 years
- Lack of a formal diagnosis of TAK
- Patients without mental capacity or willingness to provide informed consent
- Not UK based
For the physician questionnaire
- Not involved in the management/ decision making for patients diagnosed with TAK
- Not willing to take part
- Not UK based
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Patients with Takayasu Arteritis
|
An online annoymous questionnaire consisting of short-answer and multiple-choice questions
|
|
Physicians Involved in the Management of Patients with Takayasu Arteritis
|
An online annoymous questionnaire consisting of short-answer and multiple-choice questions
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Patient Perspective
Time Frame: Day 1
|
To understand the lived experiences of individuals with TAK, including their symptoms, health status post-diagnosis, treatment priorities, and concerns. The questionnaire covers the following topics:
|
Day 1
|
|
Physician Perspective
Time Frame: Day 1
|
To evaluate current clinical management strategies for TAK, identify treatment priorities, and highlight areas of unmet need in clinical practice. The physician questionnaire covers the following topics:
|
Day 1
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Vascular Diseases
- Cardiovascular Diseases
- Skin Diseases
- Skin Diseases, Vascular
- Aortic Diseases
- Vasculitis
- Arteritis
- Skin and Connective Tissue Diseases
- Aortic Arch Syndromes
- Takayasu Arteritis
- Health Care Quality, Access, and Evaluation
- Investigative Techniques
- Epidemiologic Methods
- Data Collection
- Health Care Evaluation Mechanisms
- Quality of Health Care
- Public Health
- Environment and Public Health
- Surveys and Questionnaires
Other Study ID Numbers
- 25-EMREC-064
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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