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Evaluation of a New 6 Minute Walk Test Smartphone App in Patients With Pulmonary Hypertension

Evaluation of a New 6 Minute Walk Test Smartphone App in Patients With Pulmonary Hypertension (The 6-APP Study)

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04633538
Acronym
6-APP
Enrollment
30
Registered
2020-11-18
Start date
2018-01-15
Completion date
2020-04-01
Last updated
2025-03-07

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

Conditions

Pulmonary Hypertension

Brief summary

Comparison of standard 6 minute walk test with 6 minute walk test smartphone app.

Detailed description

Pulmonary Arterial Hypertension (PAH) is a progressive illness that; if not diagnosed early or left untreated, can be a severe life limiting condition . It is a chronic disease of the pulmonary vasculature, with vascular proliferation and remodelling of the small pulmonary arteries leading to a progressive increase in pulmonary vascular resistance (PVR). This can ultimately lead to right heart failure and premature death . The predominant symptom of PAH is dyspnoea on exertion, with a decrease in exercise capacity, and most patients present with this symptom . PAH is an uncommon condition, affecting about 6000 patients in the United Kingdom , and due to its rarity, the NHS commissions 7 centres to care for patients with PAH. Oxford University Hospital NHS Foundation Trust works closely with the Royal Brompton Hospital to provide care for patients with PAH in Oxfordshire and the surrounding region. The six-minute walk test (6MWT) is a standard method for measuring exercise capacity in patients with cardiopulmonary disease such as PAH. The 6MWT measures how far a patient can walk in 6 minutes. Walking is an activity performed every day, by most patients except for those most severely limited. By assessing patients' ability to exercise, the 6MWT provides a global assessment of respiratory, cardiovascular, neuromuscular and cognitive function. The 6MWT does not differentiate what limits the patient, nor does it assess maximal exercise capacity. Instead, the 6MWT allows the patient to exercise at a daily functional level, and is a useful tool for assessing changes after a therapeutic intervention, and correlates with a subjective improvement in dyspnoea . In PAH the 6MWT is used to evaluate patients' response to treatment, with an increase in 6MWT distance of greater than 42m being considered a clinically significant improvement . Furthermore, change in 6MWT distance correlates with VO2 max (maximum rate of oxygen consumption measured during exercise), NYHA class (classification of patients' daily limitation) and mortality in PAH patients, providing an objective assessment of disease progression, prognosis and response to treatment. It is a universally accepted test as it is safe and easily performed by the patient. The 6MWT has become the primary end-point for many trials, and as a surrogate invalidated survival outcome for all placebo controlled trials of PAH therapy . It is used by regulatory bodies to determine whether a treatment should be approved. However, there is much discrepancy between whether it is the total distance walked at baseline prior to treatment, a decrease in total distance walked over time or a percentage increase in walking distance that correlates best with survival outcome. The investigators hypothesize that it is all 3 of these measures, and that having a validated and more reproducible 6MWT would help assess patients and guide treatment strategies better. The test is usually performed in hospital, by walking along a hospital corridor, where many factors on the day of the test can affect patients' performance, including tiredness, unfamiliarity with the environment or anxiety. The test typically requires 2 physiologists to monitor the distance walked by the patient, their oxygen saturations by pulse oximetry, and to record symptoms felt during the test. To improve the assessment of a patient's exercise capacity using a 6MWT, the investigators hypothesize that the test would reflect more the patient's functional status, if it were undertaken prior to the hospital outpatient appointment. The investigators have designed a mobile-phone app that allows patients to perform the 6MWT within the patient's home environment. This is felt to be more appealing to the patients, and would reduce the time spent in hospital on the day of their outpatient appointment. The 6MWT app is categorised as a mobile-health (m-health) system, a form of telehealth whereby healthcare is delivered at a distance using smartphones. By utilizing biometric collection devices such as a pulse oximeter monitor with Bluetooth capability, m-health can be used to measure the oxygen saturation levels in the blood from patients, and transmit them to a secure server, allowing them to be reviewed by cardiologists and other healthcare professionals. The evidence-base for m-health as a tool for assessing physical fitness is increasingly established. This new approach not only offers the opportunity for reliable collection of data, but provides the infrastructure to do this at scale and will allow decisions on patients' health to be based on more frequent and more accurate information. There are no known risks to undertaking a 6MWT in the community as walking is an activity of daily living, and all patients are encouraged to walk daily. The population to be studied will be those with PAH who are currently assessed with a 6MWT. Once the app has been validated, patients with any type of cardiorespiratory disease who are assessed with a 6MWT could use the app, for example patients with chronic obstructive airways disease, heart failure, renal failure, and pre-transplantation work up. The 6MWT results form part of the NHS data set collected by NHS England for patients with PAH, and it would be beneficial to have a more reproducible assessment, whose results could be compared between the 7 centres providing care for these patients. At present, there is much variability in how 6MWTs are performed between units, and the app would reduce this variability. The 6MWT has been undertaken at the John Radcliffe hospital for 5 years and the investigators will also retrospectively analyse the data from the 6MWT that have previously been undertaken. The data on patients will be pseudo-anonymised, i.e. no personal information like name, surname or address, will be used, but the investigators will keep date of birth, gender, diagnosis, dates and results of the 6MWT, date and causes of death. As part of the clinical care team, reviewing the data is part of the normal standard of care for patients with PHT. The data is collected on the Solus cardiac reporting system and can be extracted from this database. The data will be pseudo-anonymised by the Principle Investigator for analysis, and then shared with the wider research team. The data will be analysed to look at distance walked, and change in oxygen saturation and heart rate during the test. The investigators will analyse the data over time, to look for changes in these parameters and correlate these with outcome data, i.e. mortality. The study aims at demonstrating that patients are able and willing to use the app for the 6MWT and the measurements obtained by the app are comparable to the ones obtained in hospital.

Interventions

DEVICE6MWT smartphone app

Use of smartphone app to measure 6 minute walk test (6MWT)

Sponsors

University of Oxford
CollaboratorOTHER
Oxford University Hospitals NHS Trust
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Participant is willing and able to give informed consent for participation in the study * Male or Female, aged 18 years or above * Diagnosed with PAH who are able to undertake 6MWT off-oxygen * Being of PAH group 1 or 4 * Participant owns a compatible smartphone (Android or iPhone) and is able to use it.

Exclusion criteria

* Long term oxygen therapy * Cognitive impairments * Rheumatological diseases that limit the measurement of finger Oxygen saturations * PAH groups 2, 3 or 5 * Cannot use a smartphone * Pregnancy.

Design outcomes

Primary

MeasureTime frameDescription
Percentage of Participants Who Perform App-based Home 6MWT6 monthsPercentage of participants who perform app-based home 6MWT.

Secondary

MeasureTime frameDescription
Difference in Walked Distance Between 6MWT Test at the Clinic as Measured by Physiologists and the App in Indoor ModeAt start, at month 3 and at month 6.Comparison of the indoor app-based 6MWD against simultaneous clinic 6MWD: mean and standard deviation of the difference in distance as measured by physiologists and the app. Differences at 3 time points (start, month 3 and month 6) are lumped together in the calculation of the statistics (mean and standard deviation).
Difference in Walked Distance Between 6MWT Test as Measured by Physiologists at the Clinic and App in Outdoor Mode at the CommunityClinic tests at start, at month 3, at month 6. Community tests undertaken within 7 days of clinic test.Comparison of pairs of 6MWT distance estimates where one is the result of an observation done by a physiologist in a clinic (start, month 3 and month 6) and the other is measured by the app during an outdoor test performed within 7 days of the physiologist's observation. Measurements at 3 time points (start, month 3 and month 6) are lumped together in the calculation of the statistics (mean and standard deviation).
Test-Retest Reliability of Community-Based 6MWT6MWT in the community, at the patient's discretion (recommended once/month), over 6 monthsIntraclass correlation of app-base tests in outdoor mode in the community, measured over pairs of outdoor tests performed by the same patient no more than 7 days apart.
Compliance to Monitoring Regime in the CommunityAt month 6Percentage of patients who performed at least 1 app-based 6MWT in the community per month

Countries

United Kingdom

Participant flow

Participants by arm

ArmCount
6MWT App Group
Patients who received the 6MWT app and performed tests at the clinic and in the community using the app
30
Total30

Withdrawals & dropouts

PeriodReasonFG000
Overall StudyDeath1
Overall StudyLost to Follow-up3
Overall StudyWithdrawal by Subject1

Baseline characteristics

Characteristic6MWT App Group
Age, Categorical
<=18 years
0 Participants
Age, Categorical
>=65 years
7 Participants
Age, Categorical
Between 18 and 65 years
23 Participants
Age, Continuous50 years
Race and Ethnicity Not Collected— Participants
Sex: Female, Male
Female
11 Participants
Sex: Female, Male
Male
19 Participants

Adverse events

Event typeEG000
affected / at risk
deaths
Total, all-cause mortality
1 / 30
other
Total, other adverse events
0 / 30
serious
Total, serious adverse events
0 / 30

Outcome results

Primary

Percentage of Participants Who Perform App-based Home 6MWT

Percentage of participants who perform app-based home 6MWT.

Time frame: 6 months

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
6MWT App GroupPercentage of Participants Who Perform App-based Home 6MWT30 Participants
Secondary

Compliance to Monitoring Regime in the Community

Percentage of patients who performed at least 1 app-based 6MWT in the community per month

Time frame: At month 6

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
6MWT App GroupCompliance to Monitoring Regime in the Community12 Participants
Secondary

Difference in Walked Distance Between 6MWT Test as Measured by Physiologists at the Clinic and App in Outdoor Mode at the Community

Comparison of pairs of 6MWT distance estimates where one is the result of an observation done by a physiologist in a clinic (start, month 3 and month 6) and the other is measured by the app during an outdoor test performed within 7 days of the physiologist's observation. Measurements at 3 time points (start, month 3 and month 6) are lumped together in the calculation of the statistics (mean and standard deviation).

Time frame: Clinic tests at start, at month 3, at month 6. Community tests undertaken within 7 days of clinic test.

Population: Difference of 6MWT distances, between conventional 6MWT in clinic, and using the app in outdoor mode in the community, within 7 days from clinic 6MWT

ArmMeasureValue (MEAN)Dispersion
6MWT App GroupDifference in Walked Distance Between 6MWT Test as Measured by Physiologists at the Clinic and App in Outdoor Mode at the Community2.45 metreStandard Deviation 47
Secondary

Difference in Walked Distance Between 6MWT Test at the Clinic as Measured by Physiologists and the App in Indoor Mode

Comparison of the indoor app-based 6MWD against simultaneous clinic 6MWD: mean and standard deviation of the difference in distance as measured by physiologists and the app. Differences at 3 time points (start, month 3 and month 6) are lumped together in the calculation of the statistics (mean and standard deviation).

Time frame: At start, at month 3 and at month 6.

Population: 6MWT distances differences between conventional 6MWT in clinic, and using the app in indoor mode, simultaneously

ArmMeasureValue (MEAN)Dispersion
6MWT App GroupDifference in Walked Distance Between 6MWT Test at the Clinic as Measured by Physiologists and the App in Indoor Mode14.6 metreStandard Deviation 75.48
Secondary

Test-Retest Reliability of Community-Based 6MWT

Intraclass correlation of app-base tests in outdoor mode in the community, measured over pairs of outdoor tests performed by the same patient no more than 7 days apart.

Time frame: 6MWT in the community, at the patient's discretion (recommended once/month), over 6 months

Population: Pairs of outdoor tests performed by the same patient no more than 7 days apart

ArmMeasureValue (NUMBER)
6MWT App GroupTest-Retest Reliability of Community-Based 6MWT0.91 ICC

Source: ClinicalTrials.gov · Data processed: Feb 15, 2026