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Digitalizing multidisciplinary pulmonary rehabilitation in COPD with a smartphone application: an international observational pilot study

Authors Rassouli F, Boutellier D, Duss J, Huber S, Brutsche MH

Received 6 August 2018

Accepted for publication 6 November 2018

Published 23 November 2018 Volume 2018:13 Pages 3831—3836

DOI https://doi.org/10.2147/COPD.S182880

Checked for plagiarism Yes

Review by Single-blind

Peer reviewers approved by Dr Cristina Weinberg

Peer reviewer comments 3

Editor who approved publication: Dr Richard Russell


Frank Rassouli,1 David Boutellier,2 Jonas Duss,2 Stephan Huber,2 Martin H Brutsche1

1Lung Center, Department of Internal Medicine, Cantonal Hospital St Gallen, St Gallen, Switzerland; 2Kaia Health GmbH, Munich, Germany

Background: Concerning COPD, pulmonary rehabilitation (PR) has a positive effect on disease progression and mortality, is cost-effective, and is a part of recommendations of international guidelines. Only a minority of patients profit from conventional PR due to a lack of resources, physicians’ guideline adherence, or patients’ motivation. Novel digital therapies like Kaia COPD, a smartphone application that digitizes PR in COPD, are promising solutions to fill this void.
Methods: Kaia COPD provides a digital version of PR and is certified as a class-I medical device in the European Union. We investigated anonymized data from users of the Kaia COPD app on in-app retention and the change in health-related quality of life (COPD assessment test and Chronic Respiratory Disease Questionnaire [CRQ]) during a period of 20 exercise days with the app.
Results: Of 349 app downloads, 56 users fulfilled inclusion criteria and 34 (61%) had finished day 20 at the time of analysis and were included. Users took 33±11 days to complete the 20-day core program. Users finishing the program reduced their COPD assessment test scores (mean 2.5 units from 21.6±7.7 to 19.1±8.4 units, P=0.008). In finishers, there was a statistically significant effect above the minimum clinically important threshold of the CRQ score on the domains of fatigue, mastery, and emotional function. There was a statistically significant but not clinically relevant effect on the domain of dyspnea of CRQ.
Conclusion: Digitalizing PR with a smartphone app is feasible and accepted by selected patients. The app leads to short-term improvement of health-related quality of life in patients completing a 20-day core program. Due to its observational character, this study has several methodological limitations and was intended to show the feasibility and to extrapolate effect sizes for planned prospective randomized-controlled trials to confirm these findings.

Keywords: COPD, pulmonary rehabilitation, telehealth care, telerehabilitation
 

Introduction

COPD is a widespread disease with an estimated global prevalence of 11.7%, which is characterized by persistent respiratory symptoms and a chronic obstructive airflow limitation, usually caused by chronic exposure to noxious inhaled agents.1 COPD is predicted to become the third leading cause of death and disability by 2030, accounting for 8.6% of deaths worldwide, and the burden of chronic diseases linked to smoking, aging, and ambient air pollution will further increase.6 Due to the high prevalence, mortality, and morbidity, COPD will be one of the biggest public health challenges in the next century.7,8 To minimize the burden of COPD for the health care system, three cornerstones can be defined: smoking cessation, reduction of acute exacerbations, and comorbidity management.7 Pulmonary rehabilitation (PR) combines these aspects in an integrative intervention in combination with muscle training.

Because respiratory and limb muscle dysfunction have been recognized as indicators for disease progression independent of lung function,9 physical exercise has become an indispensable measure to invert skeletal muscle dysfunction,10 improve exercise capacity and health-related quality of life (HRQoL), and reduce exacerbations.

PR has a positive effect on disease progression and mortality, is cost-effective, and is an important part of recommendations of international guidelines for symptomatic patients with COPD. However, even in spite of these recommendations, it often remains underutilized in clinical routine.11 Novel digital therapies have been found to be valid solutions to face this shortage.12

Objectives

The objective of this international observational pilot study is to measure the feasibility and effects of a digitalized PR program (Kaia COPD) delivered on a smartphone on HRQoL. The instruments used to accomplish this are two self-administered, validated questionnaires – the COPD Assessment Test (CAT) and the Chronic Respiratory Disease Questionnaire (CRQ)-SAS.1316

Methods

Study design and users

This observational study analyzes user behavior and self-reported clinical parameters of COPD patients using the smartphone application Kaia COPD. The study cohort was recruited through the use of online channels in Germany, Austria, and Switzerland. These channels included COPD patient groups on Facebook as well as direct advertising through online media to specifically recruit COPD patients. Criteria for sign-up in the app were age 18 years or above, sufficient knowledge of German language, possession or access to a smartphone, and diagnosis of COPD by a physician (all self-reported in the app).

Criteria for inclusion in the study were Pro users of the app with full functionality and sign-up in the app in February and March 2018. For flow diagram of study collective, see Figure 1. Subscription costs for Pro users vary on the duration of the subscription package and range from 6.65 € to 11.66 €.

Figure 1 Flow diagram of the user database and study users.

Study recruitment took place between February and March 2018.

All participants provided an electronic informed consent for the collection and analysis of data and agreed with the data privacy statement as well as the general terms and conditions of Kaia COPD. The study was approved by the ethical review board of the regional medical authorities (Bayerische Landesärztekammer) and received a waiver due to its retrospective and anonymized design (study number 2018-094). The study was carried out in accordance with the principles of the Declaration of Helsinki.

Data collection

Data were collected online from users of the app. For self-reported parameters, both the CAT and the CRQ were used. Patients were asked to fill out a survey both at the beginning of the study period and after having completed exercise sessions on 20 different days in the app. Datasets were anonymized before scientific evaluation.

Statistical analysis

Descriptive statistics were used for patient demographics (absolute or relative numbers). Differences in scores from baseline to the end-of-study visit were compared using paired t-tests. For the comparisons of intraindividual values at baseline vs follow-up, we used Student’s t-tests. All variables were represented using mean and standard deviations. All statistical analyses were done using Microsoft Excel (version 16.13.1).

Description of the app

Kaia COPD is a multiplatform smartphone application developed by Kaia Health Software GmbH (Munich, Germany) and a CE-certified class I medical device in Europe. It is indicated for the self-management and exercise training for COPD. The software is available on the Apple App Store (iOS) and the Google Play Store. All users are being presented with a list of contraindications before signing up for the application (Table 1).

Table 1 List of contraindications as mentioned in the app

Each user’s personal health status and physical limitations are evaluated in an integrated onboarding process. The app then provides daily exercises according to the resulting user profile from a selection of relevant disciplines in PR: psychology, physiotherapy, and patient education, as recommended by international medical guidelines.14 Furthermore, users have to confirm that they are physically able to conduct the exercises and that they have no contraindications to exercise therapy.

The daily PR exercises include the following elements: 1) physical exercises for strength and mobility training delivered in short videos, 2) patient education based on established patient guidelines, and 3) mindfulness techniques for disease coping. The user is presented with one exercise per category each day but can choose whether he or she wants to complete one, two, or all three elements. A screen shot of the app is provided in Figure 2.

Figure 2 Screenshots of the Kaia COPD App.

The physical exercises were developed by the company in order to be suited for COPD patients, teachable via videos, and completed without additional training equipment than what is available in a common household (eg, chairs or water bottles). The Kaia algorithm tailors both the duration and the selection of the exercises to the specific user.

Patient education is based on the internationally validated patient guideline “Living well with COPD” and adapted to be delivered on a smartphone. Additional content, such as videos teaching the correct inhaler usage for all commonly used inhaler devices in the relevant countries, was added to the program when suitable. Patients can individually decide in a conversational interface about the depth of the content pieces. Disease progression is tracked daily with a feeling thermometer on a scale from 0 to 10, a scale already verified for COPD,5 and with a dyspnea assessment on a linear Borg scale from 0 to 10. These continuous measurements are reported to the user in a dedicated screen together with the physical activity based on the number of steps per day as recorded by the smartphones integrated pedometer. Another function is an integrated coach chat in which patients can directly talk with a dedicated Kaia COPD coach for motivational and technical questions.

Results

Patient demographics

Of 349 app downloads, a total of 56 patients entered the PR program and were included. Participants were mostly female (80%). The average CAT score was 22.4 (±7.6) points, indicating a highly symptomatic patient population. Of these, 34 (61%) finished the 20-day program and questionnaires and were included in the final analysis. Overall, there were no significant demographic differences between the initial sample including all users and participants who finished the program. For patient demographics, see Table 2.

Table 2 Demographic properties of all included patients and those who finished the 20-day program and completed the follow-up questionnaire
Note: P-values are nonpaired t-tests between groups.
Abbreviation: CAT, COPD assessment test.

Effects of the 20-day program on self-reported CAT scores

To assess the potential effects of a 20-day program of the Kaia COPD app on the CAT score, we compared baseline values with follow-up values in all patients where a follow-up score after completion of the 20-day program was available. In finishers, the CAT score declined from mean 21.6±7.7 units to 19.1±8.4 units (P=0.008, Figure 3).

Figure 3 The box-plot shows CAT scores in patients finishing the program at baseline and after completion of the 20-day program.
Abbreviations: CAT, COPD assessment test; MCID, minimum clinically important difference.

Effects of the 20-day program on self-reported CRQ scores

To assess the potential effects of a 20-day program of the Kaia COPD app on the CRQ scores, we compared baseline values with follow-up values in all patients where a follow-up score after completion of the 20-day program was available. In finishers, there was a statistically significant effect above the minimum clinically important threshold of 0.5 points on the domains of fatigue (CRQ 3.4±1 at baseline vs 4.1±1.3 after 20 exercise days, P<0.001), mastery (CRQ 4.1±1.2 at baseline vs 4.6±1.1 after 20 exercise days, P<0.001), and emotional function (CRQ 3.8±1.2 at baseline vs 4.4±1.4 after 20 exercise days, P<0.001). There was a statistically significant but not clinically relevant effect on the domain of dyspnea (CRQ 3.4±1 at baseline vs 3.2±1 after 20 exercise days, P<0.05) as the reduction remained below the minimum clinically important threshold (Figure 4).

Figure 4 The box-plot shows CRQ scores in patients finishing the program at baseline (D0) and after completion (D20) of the 20-day program in the four domains: dyspnea, fatigue, emotional function, and mastery. Mean are shown with an x and the minimum clinically important difference for the CRQ score (0.5 change from baseline) is depicted.
Abbreviations: CRQ, Chronic Respiratory Disease Questionnaire; MCID, minimum clinically important difference.

Discussion

In this international observational pilot study, we assessed feasibility and short-term effects of the digitalized PR program “Kaia COPD,” delivered on a smartphone, on HRQoL of severely symptomatic COPD patients. The low conversion rate from 349 sign-ups into 56 users is a common observation when using online channels to market health care apps (unpublished data of the authors). Roughly two-thirds of users completed a 20-day PR program as described above. We found a significant and clinically relevant improvement of the average CAT score and three out of four CRQ domains (fatigue, emotional function, and mastery) after completing the program.

Jones et al reported a mean improvement in CAT score of −2.2 points after completing a conventional PR program of 42 days duration.14 The observed reduction of −2.5 points after a 20-day digitalized PR program is, thus, a promising result for selected patients. The longitudinal course of the CAT is not only an important measure of HRQoL but is also directly linked to exacerbation risk, as shown previously by our group.17

A big meta-analysis on the effects of PR found significant and relevant improvements of all four domains of the CRQ, whereas we found comparable effects regarding fatigue, emotional function, and mastery, further supporting the usefulness of our intervention.18

A well-known problem is that the effects of PR decline after completing the program.19 Maintenance programs are able to preserve the effects.20,21 Our digitalized PR program could be an easily accessible solution to serve not only as an initial but also as a maintenance program, without burden of traveling for the patients.

Furthermore, it could offer a valid solution to face the initially mentioned problem of lack of PR capacities.11,12 In addition, it could serve as alternative for patients in remote areas. Of course, this study has limitations, mainly due to the small size, the observational pilot character, and a short duration of the intervention and potential selection bias. The longer-term effects remain to be demonstrated in future studies.

Furthermore, the study population was predominantly female, which does not reflect the usual demographic properties of COPD. Male patients are affected. This property of the study population is most likely caused by the channels with which patients were targeted and higher curiosity of female patients engage in digital self-management interventions. Similar observations have been made in scientific evaluations of self-management apps in pain medicine.22,23

Other limitations of the study mostly arise from its observational uncontrolled character. Only data of finishers could be collected, so there is a possible selection bias. Furthermore, there are only limited data available on participants’ characteristics and the diagnosis was only self-confirmed during sign-up, which clearly limits the interpretation of the data. On the contrary, this is the first available study investigating the effects of digitalized PR with real-world data and showing its potential benefit that needs to be confirmed by further studies. Of note, the study was not intended to assess the clinical efficacy of the intervention but to show the potential feasibility and extrapolate effect sizes for planned prospective and controlled studies. These studies have to be conducted to eliminate the biases arising from the methodology of this study.

Conclusion

In conclusion, in this pilot study, we observed feasibility and promising effects of a 20-day digitalized PR program on CAT and HRQoL of severely symptomatic COPD patients, which has to be confirmed by well-designed randomized-controlled trials.

Disclosure

The authors report no conflicts of interest in this work.


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