The Relating Experienced To Recalled Breathlessness Observational Study

Background

Breathlessness, the subjective sensation of breathing discomfort, is common and appears with varying severity in daily life of people across a number of diseases such as congestive heart failure, asthma and chronic obstructive pulmonary disease (COPD). Breathlessness affects nearly a quarter of people 60+ and about half of patients with serious illness.[1-3] Breathlessness gives rise to increased anxiety and depression, increased risk of hospitalization and earlier death.[4]

Clinical care relies on the patient's history based on his/her symptom recall. The recalled level of recent breathlessness is used by the health professional in order to decide on the need for further investigations and treatment. Studies have shown that the recalled intensity of breathlessness during laboratory-provoked symptoms is not the same as the actually experienced symptom in daily life.[5] Further, studies has shown lacking communication in regards to breathlessness between doctor and patients.[7] Knowledge on how recalled intensity of breathlessness differs to the actual experienced intensity during activities of daily life is limited.

Several factors may influence the recalled symptom intensity including the highest and the final experienced intensity.[8, 9] A high intensity of breathlessness at the moment of recall has been correlated with higher recalled intensity than actually experienced during the period.[10] Also, even a very small decline in cognitive status was shown to influence the differences between recalled and experienced symptoms.[10]

Aims The primary aim is to evaluate the relationship between experienced breathlessness and 1) recalled (remembered) breathlessness; and 2) predicted future breathlessness. Secondary aims are to identify factors that influence the difference between experienced and recalled or predicted breathlessness, estimate the influence of breathlessness on physical activity.

Research questions.

Three types of breathlessness measures evaluated: experienced (at a time point), recalled (remembered) and predicted (future) breathlessness. The main research questions are:

1. How is the recalled breathlessness intensity for a time period (T1) related to: 1.1. Experienced breathlessness intensity during T1 measured as:

• Mean experienced intensity?
• Peak experienced intensity?
• Most recent experienced intensity
• Perceived self-efficacy related to the breathlessness
• Personality trait of high symptom sensitivity at baseline
• Experienced trajectory of breathlessness (including constant; variable; increasing; decreasing; quick change) 1.2. Predicted breathlessness intensity for a future time period (T2)

1. How is the predicted breathlessness intensity for a subsequent time period (T2) related to: 2.1 Experienced breathlessness intensity during T1? 2.2 Recalled breathlessness intensity during T1? 2.3 Experienced breathlessness intensity during T2?
2. Which factors are associated with the difference score between: 3.1 Experienced and recalled breathlessness intensity during T1? 3.2 Predicted and experienced breathlessness intensity during T2?
3. Which breathlessness measures are related to physical activity prospectively measured during a time period (T2): [Clinical sub study]

• Experienced intensity before T2?
• Recalled intensity before T2?
• The participant's predicted intensity of breathlessness for T2?

1. How do people think when they recall breathlessness over a defined time period (such as 'now', 'last 24 hours' and 'the last week')? [Clinical sub study]

Study procedures

Recruitment Potential participants will be identified by clinical and research staff at the centers of the participating investigators including primary care and internal medicine/cardiology departments in Blekinge, Örebro, and Skane University Hospital (Lund/Malmö). Participants will also be recruited through advertisements in national and local newspapers and magazines including those of the Swedish Respiratory Society, the Swedish Heart-Lung Foundation and the Heart-Lung Association, and on web-portals/sites.

Eligibility and Consent

Eligibility according to the inclusion and exclusion criteria, consent and study data are self-entered by the participant using an application on smart phone/pad.

Patients at the study centers who give their informed written consent will also be included in a clinical sub study, where additional data will be obtained on cognitive status, physical activity (using an activity monitor worn for one week), and from medical records, interview and registry follow-up.

Application based data collection

Baseline data will be recorded when starting the application and daily start and stop times will be set. At regular intervals during each day, the application will que the participant, using sound and homepage notifications, to self-rate the intensity of breathlessness during the last 10-15 minutes. Each que can be ignored or filled in at a later time. Recall of breathlessness during the preceding night or day and additional measurements are rated in the application each morning and evening, as well as for the whole week at the end of each week in the study. The participant can quit the application at any time and will be asked to complete the cessation/exit assessments for the completed part of the week. All application data, linked to the participant-specific study-ID, is encrypted and transferred to a central database in real time via the internet connection. If no Internet connection is available at the time of transfer or if for some reason the data transfer is interrupted, the data will be stored locally on the device and the application will try to resend when the connection is re-established and stabilized. The data will also be kept on the device until the end of the study to safeguard and create a redundancy. The database is located physically at Blekinge Institute of Technology and is used for several other clinical studies including Swedish National Study of Aging and Care in accordance with all relevant protocols for data security and integrity.

Clinical sub study

A subset of participants at the study centres will be asked to participate in a clinical sub study. In addition to the information regarding the main application-based study these participants will receive specific information about the sub study on paper and be asked to give their written informed consent to participate. A log of the study ID, Swedish social security number (for sub study patients only) is kept at each participating centre. Data including demographics, diagnoses, measures of pulmonary and cardiac function, treatments, and hospitalizations will be obtained from medical records and national registries with up to five years follow-up of diagnoses and hospitalizations (Patient Registry), dispensed medications (Prescribed Drug Registry) and survival (Causes of Death Registry). Participants will be asked to fill in a daily diary of the main events causing breathlessness and its impact during the day. Participants will also be invited to take part in a semi-qualitative interview focusing on their experience of breathlessness and specifically how they cognitively recall breathlessness over different time periods such as 'now', 'last 24 hours' or 'last week' using the study questionnaires and semi-structured qualitative interviews. This group of participants will also be interviewed shortly about their experiences on using the mobile application.

Power and Sample Size

To obtain a power of 80% to detect a clinically and statistically significant difference of 1 point on a 0-10 NRS between the mean experienced and the recalled daily breathlessness score, assuming a pooled standard deviation (SD) of 1.81, a minimum of 30 participants need to be included. This is consistent with the sample size of Meek et al.[11] To account for loss of data and ensure adequate power, at least 45 participants with data on 2 days or more will be included.

Ethical considerations

Informed consent to participate will be obtained from all participants, including that participation is entirely voluntary and does not affect care or clinical contacts and that participation can be discontinued at the discretion of the participant, and that upon discontinuing, no further data will be collected.

In the application, data are de-identified using a study ID number. For patients who do not participate in the clinical sub study, the Swedish social security number is not recorded. For patients in the clinical sub study, clinical data will be cross-linked with data collected through the application using a key between the study ID (used in the application) and the participant's Swedish social security number stored securely at the clinical centre.

Data will be presented on the group level only so that individual participants cannot be identified. The findings will be published in national and international peer-reviewed scientific journals. The de-identified data will be posted in open access data repository in accordance with the requirements of the scientific journal.