A Reminder App for Supporting Adherence to Treatment Goals in Parkinson's Disease

Aims:

The aim of this project is to investigate whether the use of a recently developed reminder app ApplTree improves attainment of personalised specific treatment goals in people with Parkinson's disease (PD).

Hypothesis:

The hypothesis of this study is that introduction of the reminder app will significantly improve attainment of treatment goals.

Methods

Design:

A single case experimental design (SCED) will be utilised with multiple baselines across participants with randomisation of the onset of the intervention phase for each participant.

Participants:

Participants will have a clinical diagnosis of PD. Further, the Parkinson's care team or the individual will have expressed concerns about adherence or attainment of treatment goals. Due to the design of the study, participants will be required to own a smart phone and have a partner or significant other who is able to, and consents to, monitor and support the participant's goal attainment as the nominated person.

Recruitment:

PD patients will be recruited via the movement disorder teams and movement disorder neurology clinics in Greater Glasgow and Clyde NHS Trust (GGC) via their Parkinson's consultant, named Parkinson's nurse specialist, occupational therapist, or physiotherapist within the team.

Measures:

Pre intervention measures:

All measures are validated for PD and recommended by the Movement Disorder Society (MDS).

• A cognitive screen will be completed with all participants, the Montreal Cognitive Assessment.
• Parkinson's Disease Quality of Life Questionnaire. A proxy-rating version will also be utilised.
• Prospective and Retrospective Memory Questionnaire (PRMQ). A proxy-rating version of the PRMQ will also be utilised to alleviate limitations of self-report measures and build a broader picture.
• Apathy Scale (AS).
• Currently, no measure of anxiety is recommended by the MDS, therefore, the Generalised Anxiety Disorder severity index (GAD-7) and the Patient Health Questionnaire (PHQ-9) will be used to assess emotional wellbeing.

A weekly/daily monitoring form will be used by the partner during all phases of the intervention to record completion of intended goal related tasks (e.g., taking medication on time, completing prescribed exercises, nutritional snack, attending support group).

Procedure:

The study will run in batches of three participants, with replication of the design across the second set of three. The data collection phase for each participant will vary based on completing at least 5 data points within both the baseline and intervention phase and will range from 31-43 days for each participant. It is hoped that the timeframes for goals will require at least one reminder activity per day and so a two-day period will represent one datapoint. Participants will be assigned to a baseline period of 10, 16 or 22 days and an intervention period of 21 days (3 weeks).

Schedule:

1. Members of the movement disorder teams in GGC will be asked to review caseloads for suitable participants, based on inclusion and exclusion criteria. Participants will have a diagnosis of Parkinson's disease, have a consenting partner or carer, have use of a mobile phone and have difficulty adhering to treatment goals.
2. Potential participants and their carers/partners (nominated person) will be sent out the participant information sheet by post or be given them by a member of their clinical team during a clinic appointment. Potential participants will be able to indicate their willingness to discuss participation in the research with the researcher by returning a consent to be contacted form by pre-post to the researcher directly or by emailing the researcher informing them of their agreement for contact.
3. Alternatively in cases where participant information is given in the appointment, participants can inform the clinical team member at their clinic appointment of their agreement for contact. In this instance staff will then send contact details of potential participants who have agreed for contact along to the researcher, via NHS secure email.
4. Participants and nominated persons who consent to contact will be given a phone call to discuss the study in more detail and have the opportunity to ask any questions and, if ready, make a decision on whether they would like to participate and if undecided will be given a follow up call in 2 -5 days (depending on when is convenient for them). Inclusion and exclusion criteria will also be reviewed at this point to ensure eligibility.
5. Eligible participants and nominated persons will then meet with the researcher initially to complete written consent form and pre intervention measures. This meeting will be either face-to-face in an NHS building, face-to-face in their own home or via video call, depending on participant preferences and travel limitations.
6. Participants and nominated persons will then meet with the researcher a second time (Face-to-face or Video call) to discuss and formulate specific and personalised treatment/therapy goals. Discussion of goals will be informed by pre-intervention measures, partners and participants own views. Goals will be relevant to the management and treatment of Parkinson's Disease and have a memory and motivational component such as reminders for medication regime or physical exercises.
7. A weekly monitoring form will then be given to participants' nominated person to record completion of intended goal related tasks (e.g., taking medication on time, completing prescribed exercises, nutritional snack, attending support group) and the baseline phase will begin for a duration of 10, 16 or 22 days the following day. The duration of the baseline phase will be randomly assigned using an online random number generator.
8. The nominated person will receive a weekly reminder call to ensure the weekly monitoring form is being completed and to troubleshoot any problems.
9. The nominated person will receive a reminder text on a daily basis to ensure the form is being completed daily.
10. At the end of the baseline phase, participants and partners will meet with the researcher (Face to face or video call) to receive a training session on using the app and to input reminders for specific goal related actions.
11. Participants will then start an intervention phase of 22 days and partners will continue to use the monitoring form provided.
12. Participants will receive a weekly phone call to troubleshoot any problems.
13. The nominated person will receive a reminder text on a daily basis to ensure the monitoring form is completed daily.
14. At the end of the intervention stage participants and nominated persons will meet with the researcher a final time for a debrief (face-to-face or video call).

Setting:

Meetings with participants will be in an agreed NHS building, remote video call via attend anywhere, or in some cases in the participants own home. Due to the nature of health conditions and travel limitations within the population, the preferences of the participant and their nominated person will be given priority for arranging meetings. Current Scottish government/NHS GG\&C guidance surrounding COVID-19 will also be taken into account. Telephone calls and video calls will be completed by the researcher from an NHS premises, to ensure confidentiality of data collected.

Materials:

ApplTree is a reminding app designed to be used by people with cognitive impairments as a result of acquired brain injury. ApplTree has a narrow/deep user interface design which presents a small amount of information at a time to minimise the burden on people with cognitive impairment. Each participant will download the ApplTree app onto their own smart device. The app is free to use and maintained by Glasgow University Software Services (GUSS).

Analysis Plan:

The primary outcome measure will be the percentage of goal related tasks carried out independently (i.e., without prompting from another person) per two-day period. The primary outcome is measured via the daily monitoring form, completed by participant's nominated person. In line with recommendations for analysis of SCED data, the data will be analysed through visual analysis of graphs and Tau-U analysis to determine whether a significant improvement is found between baseline and intervention phase.

Sample Size:

The Risk of Bias in N of 1 Trials (RoBiNT) recommends that SCED designs provide at least three demonstrations of the treatment effect. In a multiple baseline across participants design this means a minimum of three participants. Additionally, the RoBiNT highlights the importance of replication, referring to replication of the overall study, meaning replication of the set of three participants. Hence, the present study will aim to recruit a minimum of six participants, and to allow for possible withdrawals the aim will be to recruit nine participants.