NCT07574151

Brief Summary

People who are invited to take part in health research are usually given written information, such as invitation letters, and information sheets. These documents are essential because they help people understand what the study involves and decide whether they want to take part. However, many studies have shown that research information is often too complex, too long, or written in technical language. This can make it difficult for people to fully understand the study and give informed consent. This study aims to assess how clear, accessible, and acceptable draft research documents are for a proposed future doctoral study related to thoracic aortic disease. Thoracic aortic disease is a long-term condition that requires regular monitoring, and people in surveillance programmes may be invited to take part in research. It is therefore important that study information is clear, sensitive, and easy to understand. In this study, staff and students from the University's School of Health Sciences will be asked to review draft recruitment materials. These materials include a study invitation, an information sheet, and interview guide. Participants will be asked to give feedback on how easy the documents are to read, whether the information is clear, whether the tone feels appropriate, and whether the amount of information feels reasonable. The study will also use a standard readability tool to assess whether the documents are written at a level suitable for the public. This research does not involve patients and is considered low risk. Its purpose is to improve research materials before they are used with patients, helping to support informed consent, reduce confusion, and improve ethical and inclusive research practice in future studies.

Trial Health

77
On Track

Trial Health Score

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

Enrollment
30

participants targeted

Target at below P25 for all trials

Timeline
3mo left

Started Mar 2026

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

Study Progress38%
Mar 2026Aug 2026

Study Start

First participant enrolled

March 11, 2026

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

April 24, 2026

Completed
13 days until next milestone

First Posted

Study publicly available on registry

May 7, 2026

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 31, 2026

Expected
12 days until next milestone

Study Completion

Last participant's last visit for all outcomes

August 12, 2026

Last Updated

May 7, 2026

Status Verified

March 1, 2026

Enrollment Period

5 months

First QC Date

April 24, 2026

Last Update Submit

May 1, 2026

Conditions

Keywords

SurveillanceRecruitment materialsClarityAcceptability

Outcome Measures

Primary Outcomes (1)

  • Clarity of recruitment materials

    How well participants understand information provided

    up to 24 weeks

Study Arms (2)

Staff

Staff in the School of Health Sciences (University of Nottingham)

Other: Acceptability and Clarity

Student

Students in the School of Health Sciences (University of Nottingham)

Other: Acceptability and Clarity

Interventions

All study participants are assessing the clarity and acceptability of Recruitment Materials for a Study on Thoracic Aortic Disease Surveillance

StaffStudent

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Staff and Students within the School of Health Sciences at the University of Nottingham.

You may qualify if:

  • Individuals who are staff or students within the School of Health Sciences at the University of Nottingham.
  • Participants aged 18 years or older who can read and understand English.

You may not qualify if:

  • Individuals who are unable to provide informed consent.
  • Individuals who are unable to read or understand English

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

School of Health Sciences ( University of Nottingham)

Nottingham, United Kingdom

RECRUITING

Study Officials

  • Charles B Mensah, MA Research Methods -Health

    University of Nottingham

    STUDY DIRECTOR
  • Lesley Halliday, Dr

    University of Nottingham

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Charles B Mensah, MA Research Methods- Health

CONTACT

Study Design

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

Study Record Dates

First Submitted

April 24, 2026

First Posted

May 7, 2026

Study Start

March 11, 2026

Primary Completion (Estimated)

July 31, 2026

Study Completion (Estimated)

August 12, 2026

Last Updated

May 7, 2026

Record last verified: 2026-03

Locations