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COPD study seeks to personalize activity tracking

NCT ID NCT06330623

Knowledge-focused Sponsor: University of Leicester Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study looked at how people with COPD experience physical activity. Researchers interviewed 54 participants and had them wear activity monitors to compare standard activity levels with personalized intensity measures. The goal was to better understand how to tailor activity recommendations for individuals with COPD.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

54 people

The number who actually took part.

Started

Nov 2023

Finished

Mar 2026

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

Phase 1: Patients from the COPD nursing ward, previous research studies and pulmonary rehabilitation programme. Phase 2: Patients from the pulmonary rehabilitation programme.

Ages

40 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Phase 1: Inclusion Criteria: * Willing and able to provide informed consent for participation in the research. * The patient has a confirmed diagnosis of COPD using spirometry (based on GOLD criteria (Agustí et al., 2023). * Male or female, aged 40+ years * Able to communicate in written and spoken English. Exclusion Criteria: * Unable to provide valid informed consent. * Severe psychiatric disorders * Aged less than 40 years * Unable to understand written or spoken English. Phase 2: Inclusion Criteria: * Willing and able to provide informed consent for participation in the research. * The patient has a confirmed diagnosis of COPD using spirometry (based on GOLD criteria. * The patient is referred for PR at the UHL. * Male or female, aged 40+ years * Able to communicate in written and spoken English Exclusion Criteria: * Unable to provide valid informed consent. * Lack of motivation to participate in PR programme. * Any-contra-indications absolute or relative to exercise training. * Has had a cardiac event within last 6 weeks * Severe psychiatric disorders * Patients with a history of MRSA +ve screens (patients can be assessed and given an exercise programme but cannot attend the classes. Patients need to have 3 consecutive -ve MRSA swabs before they can attend). * Aged less than 40 years * Unable to understand written or spoken English.

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Conditions

The condition(s) this trial relates to.

chronic obstructive pulmonary disease Motor Activity

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Chronic obstructive pulmonary disease

Contacts and locations

Locations

  • NIHR Leicester Biomedical Research Centre - Respiratory

    Leicester, Leicestershire, LE67 2DU, United Kingdom

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