TARA Working Prototype Engagement Evaluation: Feasibility Study

NCT04085302 | Completed

• 1 other identifier: 0352-2133
• Study Type: interventional
• Target: 16
• Locations: 1 country
• Sites: 1

Brief Summary

TARA is a Digital Behaviour Change Intervention (DBCI) for individuals with Chronic Obstructive Pulmonary Disease (COPD)(IwCOPD), which has been designed using a Human-Centred Design (HCD) methodology. HCD involves, among other elements, members of the target audience in evaluations at multiple stages within the design process. This feasibility study is primarily designed to assess the acceptability of the DBCI test asset to the target audience. Acceptability as defined for the purpose of this study includes usability of the system, and perceived value and desirability to the end-user audience. As such, engagement in this context is deemed to mean the degree to which the test asset provides a usable, acceptable, desirable and valuable experience to its users during a time-limited trial.

Conditions

Pulmonary Disease, Chronic Obstructive

Outcome Measures

Primary Outcomes (4)

• % of study participants achieving 80% or higher engagement score with their personal TARA program

  Up to 14 days

• Study participant's motivation to engage with the TARA working prototype (version 1) and their perceptions of value and usefulness

  Qualitative assessment of motivation and perceptions of value and usefulness at different stages in the participant's journey through the prototype; data sourced via discussion in an exit interview at the end of the study.

  Up to 14 days

• Evidence of usability issues, patterns of dis-engagement or failures of use in particular pages or functional areas of the prototype

  Analysis of usage data of the site to explore if there are common points at which participants fail to progress, make mistakes or abandon interactions; Data will be sourced from individual and amalgamated usage analytics - data points will include drop-out rates for each of the main functional areas of the site and will be supplemented by within-page usage data An overall score for perceived ease-of-use will be generated using the 'System Usability Scale' (SUS), using self-reported data from the pre- and post-TARA participant questionnaire

  Up to 14 days

• Study participant's reports of usability or other issues from using the prototype

  Up to 14 days

Secondary Outcomes (3)

• % of study participants who achieve a score of 8 or greater in Knowledge, Motivation, Confidence (KMC) assessments

  Up to 14 days

• % of study participants who achieve a positive change in measures of motivation, activation, competence (self-efficacy) and stage of change

  Up to 14 days

• % of study participants who report increases in adherence to once daily inhaled medication and reduction in Chronic Obstructive Pulmonary Disease (COPD) symptoms

  Up to 14 days

Study Arms (1)

All subjects

EXPERIMENTAL

Device: Digital Behaviour Change Intervention

Interventions

Digital Behaviour Change Intervention DEVICE

14 days

All subjects

Eligibility Criteria

• Age: 40 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Signed and dated written electronic informed consent (e-consent) in accordance with International Council on Harmonisation-Good Clinical Practice (ICH-GCP) and local legislation prior to admission to the study
• Male or female patients
• All patients must have a self-reported confirmation of a physician diagnosis of Chronic Obstructive Pulmonary Disease (COPD)(or chronic bronchitis or emphysema)
• Age ≥ 40 years
• Patients must be current or ex-smokers with a smoking history of at least 10 pack-years (pack years = \[cigarettes per day/20\] x years of smoking)
• Modified Medical Research Council (mMRC) Score ≥ 1 (i.e. evidence of activity-related breathlessness)
• Patients must have a current prescription for once daily maintenance bronchodilator in keeping with their approved labels as well as a short-acting bronchodilator ("rescue medication") for at least 3 months prior to study enrolment
• Participants must be willing to use a smart watch and be willing to complete all data collection requirements (within TARA plus phone interview plus on-line questionnaires)
• Patients must confirm that his/her treating physician has been informed about the patient's participation in the study (prior to TARA log-in)
• Fluency in written English
• Currently residing in US (for duration of study)
• Not fully adherent (self-report) to once daily inhaled COPD medication (\<80% on a protocol-specific participant self-assessment scale of medication adherence (0 - 100%))
• Access to (and comfort with) a digital device (Desktop; Laptop; Tablet), with updated Firefox \[version 67.0 and above\] or Chrome \[version 75.0.3770.80 and above\] browsers installed (or willing to download up-to-date version for the study), and daily home access to internet
• Need to have personal e-mail account that is used daily

You may not qualify if:

• Patients with asthma
• Patients who are currently prescribed oxygen therapy
• Patients who have completed a pulmonary rehabilitation (PR) program in the 6 weeks prior to enrolment or patients who are currently in a PR program (rationale: PR programs typically include a self-management component which may interfere with study objectives)
• Planned vacation period during the study period that requires overnight stays away from home
• Major surgery performed within 6 weeks prior to enrolment or planned within 2 months after enrolment, e.g. hip replacement
• Previous enrolment in this study
• Currently enrolled in another investigational device or drug study/trial, or less than 30 days since ending another investigational device or drug trial(s), or receiving other investigational treatment(s)
• Women who are pregnant, nursing, or who plan to become pregnant while in the trial
• Current use of a Smartwatch and/or wrist-worn step counter and not willing to switch to the study-specific Smartwatch for the duration of study
• Any medical or neuro-cognitive condition that would limit the ability of the participant to consent

Sponsors & Collaborators

• Boehringer Ingelheim: lead

Study Sites (1)

Medullan

Somerville, Massachusetts, 02144, United States

Location

MeSH Terms

Conditions

Pulmonary Disease, Chronic Obstructive

Condition Hierarchy (Ancestors)

Lung Diseases, Obstructive; Lung Diseases; Respiratory Tract Diseases; Chronic Disease; Disease Attributes; Pathologic Processes; Pathological Conditions, Signs and Symptoms

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: NA
• Masking: NONE
• Purpose: DEVICE FEASIBILITY
• Intervention Model: SINGLE GROUP
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: September 3, 2019
• First Posted: September 11, 2019
• Study Start: September 26, 2019
• Primary Completion: December 3, 2019
• Study Completion: December 3, 2019
• Last Updated: September 11, 2020

Record last verified: 2020-09

Data Sharing

• IPD Sharing: Will not share

Locations

US (1)