NCT04404803

Brief Summary

The primary objective of this project is to understand the reasons why patients agree / disagree to take part in ophthalmology research. This will be done by asking participants to complete a Research Questionnaire.

Trial Health

43
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
1,500

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jan 2019

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
unknown

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

November 22, 2018

Completed
2 months until next milestone

Study Start

First participant enrolled

January 21, 2019

Completed
1.4 years until next milestone

First Posted

Study publicly available on registry

May 28, 2020

Completed
3.6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

January 1, 2024

Completed
Last Updated

April 26, 2023

Status Verified

April 1, 2023

Enrollment Period

4.9 years

First QC Date

November 22, 2018

Last Update Submit

April 25, 2023

Conditions

Eye Diseases

Outcome Measures

Primary Outcomes (2)

  • Assessment of motivations to participating in ophthalmology research.

    Questionnaire

    5 years

  • Assessment of barriers in participating in ophthalmology research

    Questionnaire

    5 years

Interventions

questionnaireOTHER

Patients will be asked to complete a questionnaire about the reasons why they agree / decline to take part in research.

Eligibility Criteria

Age16 Years+
Sexall
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

All individuals will be considered for inclusion in this study regardless of age, disability, gender reassignment, marriage and civil partnership, pregnancy and maternity, race, religion and belief, sex, and sexual orientation except where the study inclusion and exclusion criteria explicitly state otherwise.

You may qualify if:

  • Over 16 years old
  • Willing to participate by completing the questionnaire
  • Must be able to speak and read English

You may not qualify if:

  • Under 16 years of age
  • Not willing to complete the questionnaire

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Monika Cien

Manchester, M13 9WL, United Kingdom

RECRUITING

MeSH Terms

Conditions

Eye Diseases

Interventions

Surveys and Questionnaires

Intervention Hierarchy (Ancestors)

Data CollectionEpidemiologic MethodsInvestigative TechniquesHealth Care Evaluation MechanismsQuality of Health CareHealth Care Quality, Access, and EvaluationPublic HealthEnvironment and Public Health

Central Study Contacts

Monika Cien

CONTACT

01617011765monika.cien@mft.nhs.uk

Hannah Kindrade

CONTACT

0161 701 0566hannah.kinrade@mft.nhs.uk

Study Design

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

Study Record Dates

First Submitted

November 22, 2018

First Posted

May 28, 2020

Study Start

January 21, 2019

Primary Completion

January 1, 2024

Study Completion

January 1, 2024

Last Updated

April 26, 2023

Record last verified: 2023-04

Data Sharing

IPD Sharing
Will not share

Locations

GB(1)