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COPDC-FINDNCT06008145

COPD Case Finding In Nottingham and District: C-FIND COPD A Pilot Study

An observational study of COPD, run by Nottingham University Hospitals NHS Trust at 1 site in United Kingdom.

Active, not recruiting

Under way, not looking for participants. Everyone needed has enrolled. The study is still running.

Official record
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Trial summary

The Targeted Lung Health Check (TLHC) is currently being rolled out in many regions of the United Kingdom and has just started in Nottingham. The same cohort of people are also at high risk for Chronic Obstructive Pulmonary Disease (COPD), a lung condition often caused by smoking and leading to breathlessness and… Read more about this study

Who is it for?
Ages 40 years and olderHealthy volunteers can take part
Conditions the study is for
COPD
How many people
568 participants
Where
1 siteUnited Kingdom
Study dates
21 Sep 2023to 31 Dec 2025
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 40 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Study population: The Targeted Lung Health Check (THLC) cohort are a population that are at high risk for COPD, a lung condition often caused by smoking. This same population will be invited to undertake breathing test in order to early diagnose COPD.

Who may be able to join

  • Smoking history - either compatible with TLHC (current or ex-smoker who are high risk based on lung cancer risk scores) or if self-presenting >10 pack years (current or ex)
  • Able to provide full informed consent.

Who cannot join

  • People currently undergoing active investigation or treatment for cancer
  • Unable to provide informed consent

Trial locations and contacts

1 site in 1 country.

United Kingdom1 site
  • Nottingham University Hospitals NHS Trust

    Nottingham, Nottinghamshire, NG5 1PB

Other trials in United Kingdom

About this study

The Targeted Lung Health Check (TLHC) is currently being rolled out in many regions of the United Kingdom and has just started in Nottingham. The same cohort of people are also at high risk for Chronic Obstructive Pulmonary Disease (COPD), a lung condition often caused by smoking and leading to breathlessness and cough. This study aims to provide pilot evidence of the role of breathing tests in those who have had a Computerised Tomography (CT) scan, in order to early diagnose COPD. Currently, at diagnosis, many patients have lost 30-40% of lung function already, which is not reversible.

This study will use the Nottingham University Hospitals Trust Mobile Research Unit. The unit will follow the CT scanner route 2-3 weeks later, and people who have had a CT scan will be invited for breathing tests. Participants will also collect further information on potential treatment options for people diagnosed with COPD earlier -including smoking cessation, symptom management and general health advice (vaccinations, diet, activity and managing infections). There is also an optional blood test.

Read more

The study aims are to determine the uptake and acceptability of breathing tests in patients at high risk of COPD, and if a community based approach co-locating with TLHC can increase uptake.

A qualitative sub-study has been added to assess the opportunities or barriers for people being invited for a COPD diagnosis visit in the community. This sub-study will have a recruitment target of 20 participants. It will involve transcribed interviews. This will help determine the accessibility of the mobile research unit in use for this study.

Read the detailed description

Ever smokers, aged between 55 to 74 years are invited for a telephone risk assessment. Those who are high risk (based on validated lung cancer risk scores, which incorporate a number of variables, including age and smoking intensity) are then sequentially invited for a CT scan in a certain locality of Nottingham as part of the TLHC. As the programme is introduced the number of invites per month will increase from 500 to 1800. It is anticipated that 40 to 45% of those will take up the invite and have a CT scan. At the time of their CT scan all smokers will be offered smoking cessation.

The clinical pathway incorporates that the CT scans will be reported by Heart Lung Health , with responsible clinician - Dr O'Dowd. Patients identified as having cancer or high likelihood will be approached and commenced on a cancer diagnostic pathway. This study addresses people who are not entering this pathway.

Two-three weeks after the CT scan, the clinical team will invite people to attend for a research study to assess lung health if they have symptoms of cough, breathlessness or 2 or more courses antibiotics in the last 15 months. No further reminder will be sent. The investigators will not excluding people with COPD already and will not turn away high-risk people who self-present even if not had a CT.

The invite will include mention of when the mobile unit is open and in their locality, what the visit consists of and that participants are free to come down at a convenient time. A telephone number and e-mail will be provided if somebody contacts the investigators and would prefer to be seen in a standard research unit - an appointment will be provided. The letter will remind participants that this cannot cover broader medical issues or emergencies, where usual clinical advice should be sought.

Following informed consent, the following will occur by trained clinical research practitioners and under the support of a research nurse.

  • Questionnaires:
  • Symptom scores and information on tobacco smoking / other exposures, past medical history, medication
  • COPD Assessment Test (CAT) Quality of Life score
  • Medical Research Council (MRC) breathlessness score
  • Exacerbation frequency
  • EQ5D - Health Status
  • Observations:
  • Oximetry for heart rate and oxygen saturations
  • Height
  • Weight
  • Blood pressure
  • Postbronchodilator spirometry - salbutamol delivered by trained staff.
  • Forced Oscillation Technique (FOT)- a non-clinically used breathing test but might have a role in early detection.
  • Approach for future research and store research data obtained here / review medical records for future medicines.
  • Invite to provide a blood sample and nasal swab for early markers of COPD - optional and currently of no clinical relevance.

Those with clinical evidence of COPD will be given information by a registered Health Care professional trained to do so on:

  • COPD and what it is.
  • Need for immunisations.
  • General health education, self-management and tobacco cessation where indicated.
  • Whether further review at the surgery is required.
  • Clinical information will be fed back to primary care surgery and uploaded onto medical health records, such as SystemOne. The participant will have consented to this.

The investigators will seek feedback from participants and subsequently from the primary care clinicians.

A qualitative sub-study has been added to assess the opportunities or barriers for people being invited for a COPD diagnosis visit in the community. This sub-study will have a recruitment target of 20 participants. It will involve transcribed interviews. This will help determine the accessibility of the mobile research unit in use for this study.

Conditions
COPD
Keywords
COPD
Medical subject headings
Pulmonary Disease, Chronic Obstructive

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Proportion of people who take up the invite to attend for a C-FIND visit.

    0-100%

    Measured: 1.5 years

Secondary outcomes (17)
  1. Proportion diagnosed with COPD

    0-100%

    Measured: 1.5 years

  2. CAT COPD Quality of Life Score

    Questionnaire. Wellbeing and daily life questions, scored 0-40 points, lower better

    Measured: 1 day

  3. MRC breathlessness score

    Questionnaire, self reported breathlessness grade 1-5, lower better

    Measured: 1 day

  4. Exacerbation Frequency

    0-12/year

    Measured: 1 day

  5. EQ-5D-5L - Health Status

    Questionnaire. Self reported health scale 0-100. Greater better

    Measured: 1 day

  6. Oximetry for oxygen saturations

    75-100% Oxygen saturation

    Measured: 1 day

  7. Height

    Participant height in metres - range 1.2-2.0m

    Measured: 1 day

  8. Weight

    participant weight in Kg - range 35-180Kg

    Measured: 1 day

  9. BMI

    12-60g/m2

    Measured: 1 day

  10. Blood pressure diastolic

    40-120mmHg

    Measured: 1 day

  11. Post bronchodilator Spirometry

    Forced Expired Volume (FEV)% - range 10-140% predicted

    Measured: 1 day

  12. FOT-R (Resistance)

    cmH2O.s/l

    Measured: 1 day

  13. FOT-X (reactance)

    cmH2O.s/l

    Measured: 1 day

  14. FOT-AX (area of reactance)

    cmH2O/L

    Measured: 1 day

  15. FOT-Fres (resonant Frequency)

    Hz

    Measured: 1 day

  16. Blood pressure -systolic

    75-230mmHg

    Measured: 1 day

  17. What are the opportunities or barriers for people being invited for a COPD diagnosis visit in the community

    To assess the barriers and opportunities presented by the use of the mobile research unit

    Measured: From enrolment to the end of study

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted23 Aug 2023
  2. Study start21 Sep 2023
  3. Primary completion31 Dec 2025 (estimated)
  4. Study completion31 Dec 2025 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Cross-sectional
Enrolment
568 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06008145
Sponsor's protocol ID
23RM005
Acronym
C-FIND
Status last verified
Dec 2025
First submitted
20 Jul 2023
Last updated
19 Dec 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of COPD, run by Nottingham University Hospitals NHS Trust at 1 site in United Kingdom.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: under way, not looking for participants, as of the sponsor's last update on 19 Dec 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United Kingdom. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Proportion of people who take up the invite to attend for a C-FIND visit. (time frame: 1.5 years). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 19 Dec 2025.

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