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Trial registered on ANZCTR
Registration number
ACTRN12612001020875
Ethics application status
Approved
Date submitted
3/09/2012
Date registered
21/09/2012
Date last updated
8/04/2014
Type of registration
Prospectively registered
Titles & IDs
Public title
The effect of web-based loving-kindness meditation and light exercise on wellbeing
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Scientific title
Internet-based randomised controlled trial comparing the effect of Loving-kindness meditation (LKM) or light exercise on wellbeing and helping behaviour in UK residents
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Secondary ID [1]
281143
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Nil
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Universal Trial Number (UTN)
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Trial acronym
WWE
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Wellbeing
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Helping behaviour
287312
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Condition category
Condition code
Public Health
287649
287649
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0
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Epidemiology
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Alternative and Complementary Medicine
287650
287650
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0
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Other alternative and complementary medicine
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Mental Health
287651
287651
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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
Participants will receive web-based Loving-kindness meditation training. The course is free of charge and very easy to follow. It takes the form of an interactive learning website with instructional videos that can be accessed through a standard web browser. The course requires that 5 x 10 minute sessions are completed per week over the 1 month (4 week) intervention period.
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Intervention code [1]
285601
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Prevention
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Intervention code [2]
285743
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Lifestyle
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Intervention code [3]
285744
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Behaviour
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Comparator / control treatment
Participants will receive web-based light exercise training. The course is free of charge and very easy to follow. It takes the form of an interactive learning website with instructional videos that can be accessed through a standard web browser. The course requires that 5 x 10 minute sessions are completed per week over the 1 month (4 week) intervention period.
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Control group
Active
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Outcomes
Primary outcome [1]
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Wellbeing (Warwick-Edinburgh Mental Wellbeing Scale)
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Assessment method [1]
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Timepoint [1]
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1. Baseline
2. Post-intervention
3. Three-month follow-up
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Secondary outcome [1]
299018
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Life satisfaction (Satisfaction with life scale)
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Assessment method [1]
299018
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Timepoint [1]
299018
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1. Baseline
2. Post-intervention
3. Three-month follow-up
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Secondary outcome [2]
299019
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Mood (I-panas-sf)
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Assessment method [2]
299019
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Timepoint [2]
299019
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1. Baseline
2. Post-intervention
3. Three-month follow-up
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Secondary outcome [3]
299020
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Stress (Perceived stress scale)
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Assessment method [3]
299020
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Timepoint [3]
299020
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1. Baseline
2. Post-intervention
3. Three-month follow-up
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Secondary outcome [4]
299021
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Depression, anxiety and irritability (Irritability, depression and anxiety scale)
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Assessment method [4]
299021
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Timepoint [4]
299021
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1. Baseline
2. Post-intervention
3. Three-month follow-up
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Secondary outcome [5]
299022
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Empathic concern (Interpersonal reactivity index)
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Assessment method [5]
299022
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Timepoint [5]
299022
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1. Baseline
2. Post-intervention
3. Three-month follow-up
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Secondary outcome [6]
299023
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Perspective taking (Interpersonal reactivity index)
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Assessment method [6]
299023
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Timepoint [6]
299023
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1. Baseline
2. Post-intervention
3. Three-month follow-up
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Secondary outcome [7]
299024
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Helping behaviour (A sum of 10 GBP will be offered to the first 200 participants after the completion of the training and the post-intervention questionnaires. A choice will be given as to whether to receive the full amount in the form of Amazon vouchers or to donate all or half to a charity of their choice)
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Assessment method [7]
299024
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Timepoint [7]
299024
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1. Post-intervention
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Secondary outcome [8]
299025
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Symptoms (Illness symptoms scale)
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Assessment method [8]
299025
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Timepoint [8]
299025
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1. Baseline
2. Post-intervention
3. Three-month follow-up
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Eligibility
Key inclusion criteria
1. UK resident.
2. Fluent English speaker.
3. Aged 18+.
4. Access to internet at home or at a place where personal activities can be developed without being disturbed.
5. Able to operate a PC unaided.
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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
1. Having been instructed by GP to avoid regular physical activity.
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Study design
Purpose of the study
Prevention
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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)
Central randomisation by computer.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Simple randomization by computerised sequence generation.
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
The people administering the treatment/s
The people assessing the outcomes
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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
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
20/10/2012
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Actual
7/02/2013
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Date of last participant enrolment
Anticipated
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Actual
1/07/2013
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
240
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Accrual to date
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Final
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Recruitment outside Australia
Country [1]
4525
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United Kingdom
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State/province [1]
4525
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Throughout the country
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Country [2]
5946
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United States of America
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State/province [2]
5946
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Throughout the country
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Funding & Sponsors
Funding source category [1]
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University
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Name [1]
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Cardiff University
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Address [1]
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RACD
Research Governance Office
30-36 Newport Road
Cardiff
CF24 0DE
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Country [1]
285926
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United Kingdom
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Primary sponsor type
Individual
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Name
Julieta Galante
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Address
Cochrane Institute of Primary Care and Public Health
Cardiff University
5th Floor, Neuadd Meirionnydd
Heath Park
Cardiff
CF14 4YS
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Country
United Kingdom
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Secondary sponsor category [1]
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Individual
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Name [1]
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John Gallacher
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Address [1]
284747
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Cochrane Institute of Primary Care and Public Health
Cardiff University
5th Floor, Neuadd Meirionnydd
Heath Park
Cardiff
CF14 4YS
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Country [1]
284747
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United Kingdom
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
287953
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Cardiff University Medical School Research Ethics Committee
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Ethics committee address [1]
287953
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Cardiff University School of Medicine UHW Main Building Heath Park Cardiff CF14 4XN
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Ethics committee country [1]
287953
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United Kingdom
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Date submitted for ethics approval [1]
287953
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06/08/2012
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Approval date [1]
287953
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15/08/2012
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Ethics approval number [1]
287953
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Summary
Brief summary
We are interested in comparing two different activities that aim to help people improve their quality of life. We want to use the information collected by this study to clarify the real effectiveness of these activities. In the long run this can help to develop more effective health policies.
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Trial website
webwellbeingexperience.co.uk
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Trial related presentations / publications
Galante J, Gallacher J, Bekkers M-J, Mitchell C. Internet-based randomised controlled trial of the effect of loving-kindness meditation on wellbeing and helping behaviour. Oral presentation. E-Epi: Expanding the Horizons symposium at EuroEpi 2013, Aarhus, Denmark, 11- 14 August.
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Public notes
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Contacts
Principal investigator
Name
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Dr Julieta Galante
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Address
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Cochrane Institute of Primary Care and Public Health Cardiff University 5th Floor, Neuadd Meirionnydd Heath Park Cardiff CF14 4YS
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Country
34655
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United Kingdom
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Phone
34655
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(+44) 0800 0 273 423
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Fax
34655
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Email
34655
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[email protected]
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Contact person for public queries
Name
17902
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Julieta Galante
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Address
17902
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Cochrane Institute of Primary Care and Public Health
Cardiff University
5th Floor, Neuadd Meirionnydd
Heath Park
Cardiff
CF14 4YS
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Country
17902
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United Kingdom
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Phone
17902
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(+44) 0800 0 273 423
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Fax
17902
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Email
17902
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[email protected]
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Contact person for scientific queries
Name
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Julieta Galante
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Address
8830
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Cochrane Institute of Primary Care and Public Health
Cardiff University
5th Floor, Neuadd Meirionnydd
Heath Park
Cardiff
CF14 4YS
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Country
8830
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United Kingdom
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Phone
8830
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(+44) (0) 29 20 687 633
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Fax
8830
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Email
8830
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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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