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Developing and Testing a Model to Identify Preventive Vision Loss Among Older Patients in General Practice

Developing and Testing a Model to Identify Preventive Vision Loss Among Older Patients in General Practice (DETECT)

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07015034
Acronym
DETECT
Enrollment
460
Registered
2025-06-11
Start date
2024-05-15
Completion date
2027-07-15
Last updated
2026-08-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Age-Related Macular Degeneration, Cataract, Diabetic Retinopathy, Glaucoma, Vision Impairment and Blindness

Brief summary

In this cohort study, the investigators will test vision screenings in Danish general practice for patients over 70 years of age with minimum one chronic condition. The main outcome is detection of vision impairment and secondary outcome is detection of conditions needing ophthalmologic follow-up but not presenting vision impairment at present time.

Detailed description

Introduction: The number of people living with visual impairment is increasing. Visual impairment causes loss in quality of life and reduce self-care abilities. The burden of disease is heavy for people experiencing visual impairment and their relatives. The severity and progression of age-related eye diseases are dependent on the time of detection and treatment options, making timely access to healthcare critical in reducing visual impairment. General practice plays a key role in public health by managing preventive healthcare, diagnostics and treatment of chronic conditions. General practitioners (GPs) coordinate services from other healthcare professionals. More involvement of the primary sector could potentially be valuable in detecting visual impairment. Methods: Investigators apply the Medical Research Council framework for complex interventions to develop a primary care intervention with the GP as a key actor, aimed at identifying and coordinating care for patients with low vision. The development process will engage patients, relatives and relevant health professional stakeholders. The investigators will pilot test the feasibility of the intervention in a real-world general practice setting. The intervention model will be developed through a participatory approach using qualitative and creative methods such as graphical facilitation. The project aims to explore the potentials and limitations of general practice in relation to detection of preventable vision loss. Ethics and dissemination: Ethics approval is obtained from local authority and the study meets the requirements from the Declaration of Helsinki. Dissemination is undertaken through research papers and to the broader public through podcasts and patient organisations.

Interventions

OTHERfocus on vision impairment in older patients in general practice

GP or GP nurse carry out the three vision tests. All patients visit optician shop collaborating with the project. An ophthalmologist review data from optometrists and provide an epicrisis to general practice. In case of acute conditions, the ophthalmologist is responsible for expedient treatment. If the patient needs further control by ophthalmologist within 12 month waiting time, general practice are responsible for referring the patient.

Sponsors

University of Copenhagen
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SEQUENTIAL
Primary purpose
SCREENING
Masking
NONE

Masking description

GP's or GP nurses, optometrists and the project ophtalmologist all give their anamnesis (and potential diagnosis). Their anamnesis are blinded to each other

Eligibility

Sex/Gender
ALL
Age
70 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* +70 years * One or more chronic diseases * Are followed by GP du to chronic disease

Exclusion criteria

* Dementia diagnosis * Known eye-diseases or are currently followed by private ophtalmologist * Not able to understand Danish

Design outcomes

Primary

MeasureTime frameDescription
Recruitment feasibilityFrom invitation to participate to enrollment within 4 weeksTotal number of patients invited to participate in the study based on the exclusion sheet and the proportion of eligible patients included by GP staff
AdherenceFrom enrollment to completion of GP intervention within 3 weeks.Proportion of patients who complete the intervention elements in general practice.
AcceptabilityFrom enrollment to interview within 12 months.Patient and health providers experiences and acceptability of the DETECT intervention

Countries

Denmark

Contacts

CONTACTCatharina Thiel Sandholdt, phd
casa@sund.ku.dk+4531646460
CONTACTFrans Boch Waldorff, prof
fransw@sund.ku.dk
PRINCIPAL_INVESTIGATORFrans B Waldorff

Center for Almen Medicin, KU

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 1, 2026