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CompletedNCT02788695NISAUpdated Aug 13, 2019

The Northern Ireland Sensory Ageing Study

An observational study in Aging, sponsored by Queen's University, Belfast. Completed at 1 site in United Kingdom. Open to participants aged 20 Years to 90 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2019-08-13.

Sponsored by Queen's University, Belfast · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
842
Ages
20 Years to 90 Years
Sex
All
01

Study summary

A visual function focused add-on study to the Northern Ireland Cohort for the Longitudinal Study of Ageing (NICOLA). There are three key aims:

  1. Quantify age-related decline in a variety of visual functions within a populations based cohort.
  2. Explore the mechanisms underlying age-related visual impairments.
  3. Investigate how visual function impacts vision related quality of life.
Read the detailed description

The investigators propose to put together a battery of test to assess different aspects of visual function and apply them to two groups of participants in order to explore differences in chronological and physiological aging.

Group 1: 25 participants from each decade from 20-90. Those from 50+ will be recruited from the NICOLA study and retinal/lens images assessed to confirm normality (drusen \<63µm or clear retina, LOCS III \<1). Those younger will be recruited via advertisements in the University and targeting friends and relatives or NICOLA participants. This will enable the rate of decline with age to be calculated. Linear, bilinear, and simple nonlinear candidate functions of parameter vs. age will be applied to determine which best characterises the change.

Group 2: 250 participants NICOLA participants aged 60 will be invited to participate; only those whose ocular images confirm normality will be included. This will enable mechanisms underlying individual differences in aging to be investigated. Normal aging will be determined from group 1 analysis and participants will be able to be categorised as aging well or aging poorly. Multivariate regression analysis will be used to investigate the relationship between visual function and lifestyle and environmental factors. Principal components analysis will be used to look at the relationships between visual parameters. These participants will also be asked to complete the NEIVFQ-25, to characterise visual function related quality of life and this will be compared with their measured visual function.

Visual function parameters measured after protocol refraction will include: Photopic and mesopic visual acuity and contrast sensitivity using City Occupational acuity-plus software17, near visual acuity, reading speed and SKILL card18, MAIA microperimetry and cone dark adaptation.19 Intra-ocular scatter will be assessed using the Oculus C-quant to assess the extent to which ocular factors are degrading vision.20 Three-point vernier acuity will also be measured as this is thought to stay stable throughout life.15 Time will be taken to ensure participants receive sufficient training to produce reliable thresholds.

All study visits will occur at the Welcome-Wolfson Clinic Research Facility.

02

Conditions studied

  • Aging

Keywords

  • Visual Nonspecific
03

In context

Lead sponsor

Queen's University, Belfast is the lead sponsor of 113 studies on the registry; 14 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
20 Years to 90 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Probability sample

Study population

25 participants from each decade from 20-90. Those from 50+ will be recruited from the NICOLA study. 250 participants NICOLA participants aged 60 will be invited to participate; only those whose ocular images confirm normality will be included.

Inclusion criteria

  • No diagnosed ocular disease.
  • Non-diabetic.

Exclusion criteria

Exclusion Criteria:

  • Any diagnosed ocular disease.
  • Diabetic.
  • Cognitive impairment.
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
842 participants (actual)
Patient registry
No
Biospecimen retention
Samples with dna

Groups and cohorts

  • Group 1 - aged 20-90 years

    25 participants from each decade from 20-90. Those from 50+ will be recruited from the NICOLA study and retinal/lens images assessed to confirm normality.

  • Group 2: aged 60 years

    Group 2: 250 participants NICOLA participants aged 60 will be invited to participate; only those whose ocular images confirm normality will be included.

06

What researchers measure

Primary outcomes

  1. Rate of decline of visual function with age

    Time frame: 24 months

07

Study locations

1 site
  • NI Clinical Research Facility
    Belfast, Northern Ireland BT9 7AB, United Kingdom
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 13, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT02788695
Lead sponsor
Queen's University, Belfast
Collaborators
College of Optometrists
Responsible party
Ruth Hogg (Doctor, Queen's University, Belfast) — Principal investigator
First posted
Jun 2, 2016
Start date
Nov 2014
Primary completion
Apr 30, 2018
Completion
Dec 31, 2018
Last update
Aug 13, 2019

Study contacts

Ruth Hogg
principal investigator · Queen's University, Belfast

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Aug 2019. You cannot join it, but the record below documents what was studied.

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