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Trial registered on ANZCTR
Registration number
ACTRN12617000253303
Ethics application status
Approved
Date submitted
16/02/2017
Date registered
20/02/2017
Date last updated
13/07/2017
Type of registration
Prospectively registered
Titles & IDs
Public title
Can placebo pills improve well-being even when you know you're taking a placebo?
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Scientific title
Open-label placebo administration and well-being in healthy participants
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Secondary ID [1]
291196
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Nil
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Universal Trial Number (UTN)
U1111-1193-1778
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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:
Well-being
302101
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Sleep quality
302102
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Physical symptoms
302103
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Condition category
Condition code
Alternative and Complementary Medicine
301724
301724
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0
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Other alternative and complementary medicine
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Mental Health
301736
301736
0
0
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Studies of normal psychology, cognitive function and behaviour
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Open-label placebo administration (1 placebo pill per day versus 4 placebo pills per day) for 5 days compared to a no treatment control condition. Adherence will be assessed via self-report at follow-up after completion of the course of placebo pills (day 6).
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Intervention code [1]
297200
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Other interventions
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Comparator / control treatment
No treatment control condition - control participants will not take placebo pills and will be observation only through completion of study questionnaires
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Control group
Active
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Outcomes
Primary outcome [1]
301117
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Psychological well-being (DASS-21; Lovibond & Lovibond, 1995; WEMWBS; Tennant et al., 2007)
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Assessment method [1]
301117
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Timepoint [1]
301117
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Follow-up 6 days post-randomisation (at completion of the 5-day course of placebo pills)
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Primary outcome [2]
301118
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Sleep quality (PSQI, Buysse et al., 1989)
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Assessment method [2]
301118
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Timepoint [2]
301118
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6 days post-randomisation (at completion of the 5-day course of placebo pills)
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Primary outcome [3]
301119
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Physical symptoms (SHC; Eriksen, Ihlebaek & Ursin, 1999)
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Assessment method [3]
301119
0
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Timepoint [3]
301119
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6 days post-randomisation (at completion of the 5-day course of placebo pills)
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Secondary outcome [1]
331773
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Adherence to placebo treatment - assessed using brief self-report measures (number of pills missed, visual analog scale)
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Assessment method [1]
331773
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Timepoint [1]
331773
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6 days post-randomisation (at completion of the 5-day course of placebo pills)
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Eligibility
Key inclusion criteria
Participants will be healthy undergraduate students
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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?
Yes
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Key exclusion criteria
Lactose intolerance
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Study design
Purpose of the study
Treatment
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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)
Allocation concealment via sealed opaque envelopes
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Simple randomisation table created by computer software (Excel)
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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
Efficacy
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Statistical methods / analysis
3-way ANCOVA assessing primary outcomes across groups, controlling for baseline
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
27/02/2017
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Actual
7/03/2017
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Date of last participant enrolment
Anticipated
26/05/2017
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Actual
29/03/2017
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Date of last data collection
Anticipated
2/06/2017
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Actual
6/04/2017
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Sample size
Target
150
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Accrual to date
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Final
92
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Recruitment in Australia
Recruitment state(s)
NSW
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Recruitment postcode(s) [1]
15324
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2052 - Unsw Sydney
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Funding & Sponsors
Funding source category [1]
295641
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University
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Name [1]
295641
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University of New South Wales
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Address [1]
295641
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School of Psychology
UNSW Sydney
NSW 2052
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Country [1]
295641
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Australia
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Primary sponsor type
Individual
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Name
Dr Kate Faasse
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Address
School of Psychology
UNSW Sydney
NSW 2052
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Country
Australia
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Secondary sponsor category [1]
294480
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None
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Name [1]
294480
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Address [1]
294480
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Country [1]
294480
0
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
296958
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Ethics committee address [1]
296958
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Ethics committee country [1]
296958
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Date submitted for ethics approval [1]
296958
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Approval date [1]
296958
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10/02/2017
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Ethics approval number [1]
296958
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Summary
Brief summary
This study will investigate the role of dose in open-label placebo administration. Recent studies have found that open-label placebo treatments are effective in improving symptoms of IBS, depression, ADHD, and low-back and migraine pain. These findings suggest the possibility of generating a placebo effect without deception. Participants will be recruited to take part in a study investigating the effect of open-label placebo administration on well-being and randomly assigned to one of three conditions: no-treatment control, low dose (1 pill per day), or high dose (4 pills per day) placebo administration.
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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
72542
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Dr Kate Faasse
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Address
72542
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School of Psychology
UNSW Sydney
NSW 2052
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Country
72542
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Australia
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Phone
72542
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+61293850364
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Fax
72542
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Email
72542
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[email protected]
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Contact person for public queries
Name
72543
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Kate Faasse
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Address
72543
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School of Psychology
UNSW Sydney
NSW 2052
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Country
72543
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Australia
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Phone
72543
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+61293850364
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Fax
72543
0
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Email
72543
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[email protected]
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Contact person for scientific queries
Name
72544
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Kate Faasse
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Address
72544
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School of Psychology
UNSW Sydney
NSW 2052
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Country
72544
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Australia
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Phone
72544
0
+61293850364
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Fax
72544
0
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Email
72544
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[email protected]
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No information has been provided regarding IPD availability
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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