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Trial registered on ANZCTR
Registration number
ACTRN12619000647134
Ethics application status
Approved
Date submitted
21/04/2019
Date registered
1/05/2019
Date last updated
12/07/2023
Date data sharing statement initially provided
1/05/2019
Date results provided
12/07/2023
Type of registration
Retrospectively registered
Titles & IDs
Public title
A randomised controlled trial comparing video-assisted informed medical consent to traditional doctor patient consent for Mohs micrographic surgery.
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Scientific title
A comparison of video assisted medical consent compared to traditional doctor-patient consent for medical procedures.
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Secondary ID [1]
297983
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Nil known
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Universal Trial Number (UTN)
U1111-1231-7942
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Trial acronym
N/A
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Linked study record
N/A
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Health condition
Health condition(s) or problem(s) studied:
Skin cancer
312396
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Condition category
Condition code
Skin
310956
310956
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0
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Dermatological conditions
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Surgery
311024
311024
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0
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Surgical techniques
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Cancer
311098
311098
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0
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Non melanoma skin cancer
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Participants will watch a 6 minute video describing Mohs micrographic surgery, including the method, risks, benefits, alternatives and aftercare. Following this, they will then see their doctor to address any personal questions or concerns, however, the procedure will not be explained to them again. Adherence will be ensured through direct observation of the participants by the study personnel.
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Intervention code [1]
314200
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Treatment: Other
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Comparator / control treatment
Usual consent process of talking to their doctor as they normally would in standard practice.
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Control group
Active
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Outcomes
Primary outcome [1]
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Patient comprehension of the procedure, assessed using a 10-item knowledge questionnaire that was designed specifically for the study.
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Assessment method [1]
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Timepoint [1]
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Immediately after the consent process
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Secondary outcome [1]
369454
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Patient satisfaction, as measured using a Likert scale satisfaction survey
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Assessment method [1]
369454
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Timepoint [1]
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Immediately after the consent process
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Secondary outcome [2]
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Patient anxiety levels, as measured using the 6-item State-Trait Anxiety Inventory (STAI).
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Assessment method [2]
369456
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Timepoint [2]
369456
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Immediately before and after the consent process
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Secondary outcome [3]
369457
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Time per consultation between patient and doctor, assessed by the study personnel using a stopwatch.
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Assessment method [3]
369457
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Timepoint [3]
369457
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Time of consultation
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Eligibility
Key inclusion criteria
Patients attending the Mohs micrographic surgery clinic at Royal North Shore Hospital or The Skin Hospital who will be consented for Mohs micrographic surgery.
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Minimum age
18
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
Those who are not able to provide informed medical consent for themselves. Also those who have a visual or hearing impairment.
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Study design
Purpose of the study
Educational / counselling / training
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Sealed opaque envelopes
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Permuted block randomisation performed by computer 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
Parallel
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Other design features
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Phase
Not Applicable
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Type of endpoint/s
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Statistical methods / analysis
We calculated a sample size of 102 participants (51 per group) to detect a minimally clinically important difference of knowledge retention post consent as undertaken on a knowledge questionnaire with 80% power at 5% level of significance.
Continuous variables will be summarised using means and standard deviations, and Categorical variables will be summarised using frequencies and percentages.
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
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Actual
11/03/2019
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Date of last participant enrolment
Anticipated
10/12/2019
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Actual
4/11/2019
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Date of last data collection
Anticipated
10/12/2019
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Actual
4/11/2019
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Sample size
Target
102
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Accrual to date
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Final
102
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Recruitment in Australia
Recruitment state(s)
NSW
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Recruitment hospital [1]
13623
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Royal North Shore Hospital - St Leonards
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Recruitment hospital [2]
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The Skin Hospital (Darlinghurst) - Darlinghurst
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Recruitment postcode(s) [1]
26290
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2065 - St Leonards
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Recruitment postcode(s) [2]
26310
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2010 - Darlinghurst
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Funding & Sponsors
Funding source category [1]
302506
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Charities/Societies/Foundations
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Name [1]
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AVANT Doctors in training research grant
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Address [1]
302506
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AVANT Mutual Level 6 Tower 3/Darling Park, 201 Sussex St, Sydney NSW 2000
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Country [1]
302506
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Australia
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Primary sponsor type
Individual
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Name
Dr Rebecca Saunderson
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Address
Department of Dermatology
Royal North Shore Hospital
Reserve Road,
St Leonards
NSW, 2065
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Country
Australia
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Secondary sponsor category [1]
302414
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None
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Name [1]
302414
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Address [1]
302414
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Country [1]
302414
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Nepean Blue Mountains Local Health District Human Research Ethics Committee
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Ethics committee address [1]
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PO Box 63, Penrith, NSW, 2751
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Ethics committee country [1]
303162
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Australia
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Date submitted for ethics approval [1]
303162
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12/06/2018
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Approval date [1]
303162
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18/07/2018
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Ethics approval number [1]
303162
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HREC/18/Nepean/78
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Summary
Brief summary
The purpose of the study is to compare a new way of undertaking informed medical consent, that being with the aid of a video, to the regular way a doctor would tell you about the procedure (which is usually a conversation between the doctor and yourself). Who is it for? You may be eligible for this study if you are aged 18 or over and are attending Royal North Shore Hospital or The Skin Hospital (Darlinghurst) for Mohs micrographic surgery. Study details Participants will be randomised by chance into two groups. One group will first watch a 6 minute video about the procedure before talking with their doctor to address any questions. The other group will only talk with their doctor (usual practice). As part of this study, all participants will complete a number of questionnaires before and after the consent process. It is hoped this research will show improved patient comprehension of the risks and benefits of the procedure, enhance patient satisfaction with the consent process, lower anxiety levels and save time.
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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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Dr Rebecca Saunderson
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Address
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Department of Dermatology
Royal North Shore Hospital
Reserve Road,
St Leonards
NSW, 2065
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Country
92698
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Australia
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Phone
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+61 2 9926 7111
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Fax
92698
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Email
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[email protected]
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Contact person for public queries
Name
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Rebecca Saunderson
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Address
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Department of Dermatology
Royal North Shore Hospital
Reserve Road,
St Leonards
NSW, 2065
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Country
92699
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Australia
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Phone
92699
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+61 2 9926 7111
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Fax
92699
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Email
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[email protected]
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Contact person for scientific queries
Name
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Rebecca Saunderson
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Address
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Department of Dermatology
Royal North Shore Hospital
Reserve Road,
St Leonards
NSW, 2065
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Country
92700
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Australia
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Phone
92700
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+61 2 99267111
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Fax
92700
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Email
92700
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[email protected]
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Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
Yes
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What data in particular will be shared?
Deidentified demographics of the participants
Time of consultation, knowledge scores, satisfaction and anxiety scores.
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When will data be available (start and end dates)?
At the trial completion, no end date determined.
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Available to whom?
To interested parties
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Available for what types of analyses?
Meta analysis
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How or where can data be obtained?
csv file with data points
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What supporting documents are/will be available?
No Supporting Document Provided
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.
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