- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07479186
Impact of Aortic Diseases on Quality of Life and Work Ability (IMPACT-A)
June 5, 2026 updated by: Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Impact of Aortic Disease on Patients' Quality of Life and Working Capacity
Aortic diseases encompass a wide spectrum of congenital and acquired, acute and chronic conditions, characterized by high clinical and prognostic complexity.
The aorta plays a central role in blood flow distribution and hemodynamic modulation owing to its elastic properties, which become progressively impaired with aging and in the presence of genetic or degenerative factors.
Beyond clinical outcomes, aortic diseases lead to a marked reduction in health-related quality of life, psychological well-being, and functional capacity, with significant occupational and social consequences, thereby making multidisciplinary management necessary.
This longitudinal observational study aims to systematically assess health-related quality of life, fatigue, psychological well-being, and work ability in patients with aortic diseases, with the objective of providing objective bases for occupational risk evaluation and promoting an interdisciplinary management model that integrates clinical, psychological, and work-related aspects, thereby supporting the maintenance or recovery of work functioning.
Study Overview
Status
Recruiting
Conditions
Study Type
Observational
Enrollment (Estimated)
300
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Ivo Iavicoli, Prof
- Phone Number: + 39 0630155145
- Email: ivo.iavicoli@unicatt.it
Study Locations
-
-
RM
-
Roma, RM, Italy, 00168
- Recruiting
- Fondazione Policlinico Gemelli IRCCS
-
Contact:
- Ivo Iavicoli
- Phone Number: 0630155145
- Email: ivo.iavicoli@unicatt.it
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Probability Sample
Study Population
Patients with aortic diseases under the care of the Complex Operative Unit of Vascular Surgery at Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Description
Inclusion Criteria:
- Male and female patients with a confirmed diagnosis of aortic disease under the care of the Complex Operative Unit of Vascular Surgery of the Fondazione Policlinico Universitario Agostino Gemelli IRCCS.
- Patients aged between 18 and 70 years.
Exclusion Criteria:
- Patients younger than 18 years or older than 70 years.
- Incomplete diagnostic workup.
- Patients who have undergone surgical procedures or experienced concomitant acute events unrelated to the aorta, with a predominant and recent functional impact, that make it impossible to isolate the effect of aortic disease on return to work.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Work Ability Index (WAI) score from baseline to 12 months in patients with aortic diseases
Time Frame: 12 months
|
Work ability will be assessed using the Work Ability Index (WAI), a validated questionnaire composed of seven dimensions evaluating current work ability, work demands, health status, sickness absence, prognosis of future work ability, and psychological resources.
The total WAI score ranges from 7 to 49 points, with higher scores indicating better work ability.
The primary outcome is the change in total WAI score between baseline and the 12-month follow-up assessment.
|
12 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Ivo Iavicoli, Prof, Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
March 31, 2026
Primary Completion (Estimated)
March 31, 2028
Study Completion (Estimated)
June 30, 2028
Study Registration Dates
First Submitted
March 13, 2026
First Submitted That Met QC Criteria
March 13, 2026
First Posted (Actual)
March 18, 2026
Study Record Updates
Last Update Posted (Actual)
June 9, 2026
Last Update Submitted That Met QC Criteria
June 5, 2026
Last Verified
March 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 27010
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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.