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Trial registered on ANZCTR
Registration number
ACTRN12621000032853
Ethics application status
Approved
Date submitted
1/10/2020
Date registered
15/01/2021
Date last updated
15/01/2021
Date data sharing statement initially provided
15/01/2021
Type of registration
Retrospectively registered
Titles & IDs
Public title
Understanding Maori People's Experience with iPad App ADOC-M/P for Goal Setting in Rehabilitation
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Scientific title
Field Testing a Maori/Pacific Version of a Japanese iPad App to Support Culturally Responsive Goal Setting in Clinical Rehabilitation: A Qualitative Study
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Secondary ID [1]
302431
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Nil Known
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Universal Trial Number (UTN)
U1111-1259-0297
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Disability
319275
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Physical rehabilitation
319950
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Stroke
319951
0
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Fractures
319952
0
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Traumatic brain injury
319953
0
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Condition category
Condition code
Physical Medicine / Rehabilitation
317241
317241
0
0
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Occupational therapy
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Physical Medicine / Rehabilitation
317242
317242
0
0
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Physiotherapy
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Stroke
317884
317884
0
0
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Ischaemic
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Stroke
317887
317887
0
0
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Haemorrhagic
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Injuries and Accidents
317888
317888
0
0
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Fractures
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Neurological
317889
317889
0
0
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Other neurological disorders
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
The intervention in this study is the use of our iPad app 'ADOC-M/P' which stands for Aid for Decision-making in Occupational Choice - Maori and Pacific version. This app is an adaption of the Japanese app ADOC. The app presents a catalogue of illustrations depicting various activities which the clinician uses to facilitate the collaborative goal-setting process with the patient. The app works by allowing the patient and therapist to individually choose up to 20 goals that they would like to work towards during rehabilitation. Then the app presents the selections together so the patient and therapist can choose 5 goals to create a rehabilitation plan. There is later a section where details regarding each specific goal may be typed up (time frame, therapist in charge, specific definition of the activity.) The app then creates a pdf with the 5 selected goals which can then be printed off an signed by the therapist and the patient.
The intervention may be delivered by any person who is employed by Whanganui district health board to work with rehabilitation patients. (Such as a physiotherapist, nurse, occupational therapist, or speech/language therapist.) Goal setting with our iPad app will be conducted by the therapist as they judge clinically appropriate. The goal setting process is face-to-face between the clinician and the patient, the iPad will be passed between the therapist and patient as necessary. The duration of goal setting with the app can be as short as 15 minutes but could be as long as 2 hours depending on how the app is used. The therapist does not need to be present when the patient is selecting their goals and the patient does not need to be present when the therapist is selecting their goals either. We will ask the clinician if they have used the app with patients/a specific patient to measure adherence. We are not employing any other strategies to measure adherence.
The participating patients with or without whanau (friends/family) will attend at least one goal setting session to be eligible for the trial. Participating patients must be able to provide informed consent.
The data collection will take place in an inpatient setting after the patient has had their goal setting session. The data collection will occur immediately after the goal setting session to up to 3 weeks after goal setting.
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Intervention code [1]
318740
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Rehabilitation
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Comparator / control treatment
No control group.
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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A patient's new subjective experience with novel iPad app ADOC-M/P to be explored in a semi-structured interview with the primary investigator and analysed by thematic analysis in NVivo.
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Assessment method [1]
325300
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Timepoint [1]
325300
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Immediately after completion of goal setting with the intervention.
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Secondary outcome [1]
387443
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Change in patient's perception of patient-clinician relationship to be enquired about in a semi-structured interview with the primary investigator and analysed by thematic analysis in NVivo.
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Assessment method [1]
387443
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Timepoint [1]
387443
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Immediately after to up to 3 weeks after completion of goal setting with the intervention.
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Secondary outcome [2]
387444
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Change in the goals set during goal setting for rehabilitation to be enquired about in a semi-structured interview with the primary investigator and analysed by thematic analysis in NVivo
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Assessment method [2]
387444
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Timepoint [2]
387444
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Immediately after to up to 3 weeks after completion of goal setting with the intervention.
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Secondary outcome [3]
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Health professionals' experiences with using the app to be enquired about in a semi-structured interview with the primary investigator and analysed by thematic analysis in NVivo
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Assessment method [3]
389471
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Timepoint [3]
389471
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1 to 3 months after receiving the app to use.
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Eligibility
Key inclusion criteria
A health professional is eligible to participate in the study if they are employed with Whanganui DHB as a health professional and if their work involves goal setting with patients.
Patients may participate if they:
• Are an adult over 16 years of age
• Identify as Maori
• Are a rehabilitation patient receiving care at Whanganui DHB (e.g. after a stroke, head injury, fractures, or other health problems.)
• Can provide informed consent
• Can communicate in English
• Can see with or without corrective lenses
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Minimum age
16
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Participants will be excluded if they:
• Score less than 8 on the MMSE (Mini Mental State Exam)
• Are discharged from the hospital before data collection and are unable to return to the hospital for an interview
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Study design
Purpose of the study
Educational / counselling / training
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Allocation to intervention
Non-randomised trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Allocation was not concealed.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
Open (masking not used)
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Who is / are masked / blinded?
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Intervention assignment
Single group
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Other design features
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Phase
Not Applicable
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
30 to 90 minute interviews with participants to be transcribed and analysed in NVivo via thematic analysis.
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Recruitment
Recruitment status
Recruiting
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Date of first participant enrolment
Anticipated
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Actual
29/10/2020
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Date of last participant enrolment
Anticipated
29/01/2021
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Actual
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Date of last data collection
Anticipated
29/01/2021
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Actual
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Sample size
Target
12
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Accrual to date
2
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Final
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Recruitment outside Australia
Country [1]
23035
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New Zealand
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State/province [1]
23035
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Whanganui/Manuwatu
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Funding & Sponsors
Funding source category [1]
306849
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University
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Name [1]
306849
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University of Otago, Wellington
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Address [1]
306849
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23 Mein Street
Newtown
Wellington
6242
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Country [1]
306849
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New Zealand
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Funding source category [2]
306877
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Charities/Societies/Foundations
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Name [2]
306877
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Royal Society Te Aparangi
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Address [2]
306877
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11 Turnbull Street
Thorndon
Wellington
6011
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Country [2]
306877
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New Zealand
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Primary sponsor type
University
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Name
University of Otago, Wellington
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Address
23 Mein Street
Newtown
Wellington
6242
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Country
New Zealand
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Secondary sponsor category [1]
307431
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None
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Name [1]
307431
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Address [1]
307431
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Country [1]
307431
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
307011
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Southern Health and Disability Ethics Committees
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Ethics committee address [1]
307011
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Ministry of Health Health and Disability Ethics Committees PO Box 5013 Wellington 6140
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Ethics committee country [1]
307011
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New Zealand
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Date submitted for ethics approval [1]
307011
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30/06/2020
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Approval date [1]
307011
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28/09/2020
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Ethics approval number [1]
307011
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Summary
Brief summary
This study aims to investigate the experiences of patients and health professionals with our iPad app ADOC-M/P. ACOD-M/P stands for Aid for Decision making in Occupational Choice - Maori and Pacific. This app is a Maori and Pacific adaption of a Japanese app called ADOC. ADOC-M/P presents a range of illustrations depicting various activities. These illustrations can be selected to represent goals for the patient and health professional to work towards in rehabilitation. We are expecting that our app will help the health professional communicate with the patient during goal setting in rehabilitation. From this, we are hoping that the patient and health professional can set meaningful goals to work towards during rehabilitation.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Miss Kato Robina McDonald
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Address
105734
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University of Otago, Wellington
23 Mein Street
Newtown
Wellington
6242
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Country
105734
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New Zealand
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Phone
105734
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+64 0272840605
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Fax
105734
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Email
105734
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[email protected]
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Contact person for public queries
Name
105735
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Kato Robina McDonald
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Address
105735
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University of Otago, Wellington
23 Mein Street
Newtown
Wellington
6242
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Country
105735
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New Zealand
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Phone
105735
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+64 0272840605
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Fax
105735
0
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Email
105735
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[email protected]
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Contact person for scientific queries
Name
105736
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Kato Robina McDonald
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Address
105736
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University of Otago, Wellington
23 Mein Street
Newtown
Wellington
6242
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Country
105736
0
New Zealand
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Phone
105736
0
+64 0272840605
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Fax
105736
0
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Email
105736
0
[email protected]
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Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
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No/undecided IPD sharing reason/comment
To protect patient confidentiality we will not release the raw transcript data to the public even after it has been de-identified. As there may still be events described in the transcripts that may identify individuals.
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What supporting documents are/will be available?
No Supporting Document Provided
Doc. No.
Type
Citation
Link
Email
Other Details
Attachment
9349
Study protocol
[email protected]
380669-(Uploaded-01-10-2020-09-17-02)-Study-related document.docx
9350
Informed consent form
[email protected]
380669-(Uploaded-01-10-2020-09-14-34)-Study-related document.docx
9351
Ethical approval
[email protected]
380669-(Uploaded-01-10-2020-09-14-34)-Study-related document.pdf
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
Download to PDF