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Trial registered on ANZCTR
Registration number
ACTRN12612000850875
Ethics application status
Approved
Date submitted
25/06/2012
Date registered
13/08/2012
Date last updated
24/06/2014
Type of registration
Prospectively registered
Titles & IDs
Public title
New horizons for weight loss using mobile technologies
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Scientific title
Acceptability and efficacy of a weight loss programme for overweight adults delivered via SMS and the Internet: a non-randomized pilot study
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Secondary ID [1]
280200
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TBF-MC11-001R (The Bupa Foundation)
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Universal Trial Number (UTN)
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Trial acronym
Horizon Study
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Overweight / obesity
286137
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Condition category
Condition code
Diet and Nutrition
286330
286330
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0
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Obesity
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Public Health
287041
287041
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0
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Health promotion/education
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
A prototype mHealth (mobile phone and internet-delivered) weight management programme. The programme will be delivered to participants for 8 weeks. Topics covered include nutritional and physical activity information and behavioural support. Text messages will be sent via mobile phone 3 times daily for the first 1-2 weeks, then twice daily for the remainder of the programme. Additionally, a few data collection question texts will be sent to participants. Participants are able to log on to the study website as they wish (this is not a requirement of the study). On the website, participants can view their individual progress compared with the group, as well as view and contribute to an online blog, and view other study resources (also provided hard copy to participants).
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Intervention code [1]
284528
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Behaviour
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Intervention code [2]
285120
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Lifestyle
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Comparator / control treatment
None
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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Potential efficacy of mHealth programme as measured by weight change from baseline (using calibrated Salter scales).
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Assessment method [1]
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Timepoint [1]
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12 weeks
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Secondary outcome [1]
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Average recruitment rate
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Assessment method [1]
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Timepoint [1]
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12 weeks
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Secondary outcome [2]
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Pilot participant demographics (age, sex, ethnicity, income, household composition, area of residence) as compared with general population demographics. Participant demographic information will be self-reported and collected using a data collection form at the baseline visit.
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Assessment method [2]
296680
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Timepoint [2]
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Baseline visit
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Secondary outcome [3]
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Participant retention rates (including withdrawal and loss to follow-up rates)
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Assessment method [3]
296681
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Timepoint [3]
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12 weeks
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Secondary outcome [4]
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Feedback from participants receiving the programme. This data will be self-reported and collected using a data collection form at the 12 week visit.
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Assessment method [4]
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Timepoint [4]
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12 weeks
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Eligibility
Key inclusion criteria
Adults aged 18 years and older who have a BMI >= 25 kg/m2 and want to lose weight. Participants also need to have internet access and own a mobile phone capable of receiving texts (SMS).
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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 cannot read or understand English.
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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)
Participants will be recruited using advertising in community venues such as libraries, community centres and GP practices, and local newspapers. Volunteers responding to advertisements will receive study information and an appointment to attend a baseline assessment where written informed consent will be obtained if the person is willing to take part.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
N/A - non-randomised pilot study
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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
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
1/09/2012
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Actual
3/09/2012
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Date of last participant enrolment
Anticipated
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Actual
28/09/2012
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
50
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Accrual to date
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Final
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Recruitment outside Australia
Country [1]
4216
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New Zealand
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State/province [1]
4216
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Funding & Sponsors
Funding source category [1]
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Charities/Societies/Foundations
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Name [1]
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The Bupa Foundation
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Address [1]
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Bupa House
15-19 Bloomsbury Way
London
WC1A 2BA
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Country [1]
284948
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United Kingdom
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Primary sponsor type
University
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Name
National Institute for Health Innovation, The University of Auckland
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Address
Level 4, School of Population Health
Tamaki Campus
University of Auckland
261 Morrin Road
Glen Innes
Auckland
1072
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Country
New Zealand
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Secondary sponsor category [1]
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None
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Name [1]
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Address [1]
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Country [1]
283821
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Other collaborator category [1]
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University
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Name [1]
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Queen Mary University of London
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Address [1]
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Wolfson Institute of Preventive Medicine,
Mile End Road
London
E1 4NS
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Country [1]
260649
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United Kingdom
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Other collaborator category [2]
260650
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University
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Name [2]
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Deakin University
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Address [2]
260650
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Centre for Physical Activity and Nutrition
221 Burwood Highway
Burwood
Melbourne
Victoria
3125
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Country [2]
260650
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Upper South B Regional Ethics Committee
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Ethics committee address [1]
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c/- Ministry of Health 6 Hazeldean Road Level 1 Montgomery Watson Building Addington Christchurch 8024
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Ethics committee country [1]
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New Zealand
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Date submitted for ethics approval [1]
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29/02/2012
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Approval date [1]
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13/03/2012
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Ethics approval number [1]
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URB/12/EXP/010
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Summary
Brief summary
This feasibility study aims to develop and pre-test an mHealth weight loss programme. 50 volunteers will be recruited from the community and given the prototype programme for 8 weeks. The programme will use mobile phones and internet to provide information (e.g related to nutrition and physical activity) and behavioural strategies to achieve weight loss and maintain a long-term healthy lifestyle. The primary aim is to evaluate the potential effectiveness of the programme (as measured by weight loss at 12 weeks).
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Trial website
Address will be: www.horizonstudy.org.nz
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Trial related presentations / publications
Methods paper in press: Wilma Waterlander, Robyn Whittaker; Hayden McRobbie; Enid Dorey; Kylie Ball; Ralph Maddison; Katie Myers Smith; David Crawford; Yannan Jiang; Yulong (Helen) Gu; Jo Michie; Cliona Ni Mhurchu. Development of an evidence-based mHealth weight management programme using a formative research process. JMIR mHealth and uHealth (in press).
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Public notes
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Contacts
Principal investigator
Name
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A/Prof Cliona Ni Mhurchu
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Address
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National Institute for Health Innovation The University of Auckland Private Bag 92019 Auckland 1142
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Country
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New Zealand
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Phone
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+64, 9, 923 4494
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Fax
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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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Associate Professor Cliona Ni Mhurchu
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Address
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National Institute for Health Innovation
The University of Auckland
Private Bag 92019
Auckland
1142
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Country
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New Zealand
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Phone
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+64, 9, 923 4494
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Fax
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+64, 9, 373 1710
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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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Associate Professor Cliona Ni Mhurchu
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Address
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National Institute for Health Innovation
The University of Auckland
Private Bag 92019
Auckland
1142
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Country
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New Zealand
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Phone
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+64, 9, 923 4494
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Fax
8140
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+64, 9, 373 1710
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Email
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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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