- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00836459
Sheffield Physical Activity Booster Trial (Booster)
December 1, 2014 updated by: Richard Hudson
A Randomised Controlled Trial and Cost-effectiveness Evaluation of "Booster" Interventions to Sustain Increases in Physical Activity in Middle-aged Adults in Deprived Urban Neighbourhoods.
Adults that increase their physical activity can improve their health, and reduce future risks to health, but long-term changes are difficult to sustain.
This study assesses whether it is worth providing further support, 3 months after giving initial advice, to those who have managed to do more physical activity.
All participants will initially be given an interactive DVD.
A researcher from Sheffield Hallam University will provide two telephone follow ups at one month intervals to assess physical activity levels.
Only those that have increased their physical activity at this point will remain in the study.
These participants will receive a "mini booster", a "full booster" or no booster.
The "mini booster" consists of a two telephone calls one month apart to discuss physical activity and usage of the DVD.
A "full booster" consists of a face-to-face meeting with the facilitator at the same intervals.
The purpose of these booster sessions is to help the individual to maintain their increase in physical activity.
The investigators will measure the differences in physical activity, quality of life and costs, associated with the booster interventions, 3 months and 9 months from randomisation.
The research will be carried out in 20 of the most deprived neighbourhoods in Sheffield.
These locations have large, ethnically diverse populations, high levels of economic deprivation, low levels of physical activity, poorer health and shorter life expectancy.
Participants will be recruited through general practices and community groups, as well as by postal invitation to ensure the participation of minority ethnic groups and those with lower levels of literacy.
Sheffield City Council and Primary Care Trust fund a range of facilities and activities to promote physical activity and variations in access to these between neighbourhoods will make it possible to examine whether the effectiveness of the intervention is modified by access to community facilities.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
282
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
South Yorkshire
-
Sheffield, South Yorkshire, United Kingdom, S10 2BP
- Centre for Sport and Exercise Science, Sheffield Hallam University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
40 years to 64 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Residents of the 20 most deprived neighbourhoods in the city of Sheffield
- Aged 40 to 64 years
- Not achieving the current recommended activity level (30 mins of moderate activity on at least 5 days) assessed using the SPAQ (Lowther, 1999) and wishing to have support to become more active
Exclusion Criteria:
- Have increased their physical activity level by at least 30 mins of moderate or vigorous activity per week (assessed using the SPAQ) since initial assessment of activity level
- Capacity to give written informed consent to trial participation
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Control
|
|
|
Experimental: Mini Booster
|
Two telephone-based physical activity consultations, delivered in a motivational interviewing style, at one month and two months from randomisation
|
|
Experimental: Full Booster
|
Two face-to-face physical activity consultations, delivered in a motivational interviewing style, at one month and two months from randomisation
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Physical activity measured by accelerometry.
Time Frame: 3 months post-randomisation
|
3 months post-randomisation
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Physical activity assessed by accelerometry.
Time Frame: 9 months post-randomisation
|
9 months post-randomisation
|
|
Self-reported moderate or strenuous physical activity using the Scottish Physical Activity Questionnaire (SPAQ, incorporating Stage of Change information) which records type and duration of activities in the previous week
Time Frame: 3 months and 9 months post-randomisation
|
3 months and 9 months post-randomisation
|
|
Health-related quality of life using the Sheffield Version SF-12v2 plus 4 survey instrument
Time Frame: 3 months and 9 months post-randomisation
|
3 months and 9 months post-randomisation
|
|
Self-reported use of community facilities for physical activity
Time Frame: 3 months and 9 months post-randomisation
|
3 months and 9 months post-randomisation
|
|
Self-reported health and social care contacts
Time Frame: 3 months and 9 months post-randomisation
|
3 months and 9 months post-randomisation
|
|
Psychological measures of motivation, assessed using BREQ-2 (Mullan et al, 1997)
Time Frame: 3 months and 9 months post-randomisation
|
3 months and 9 months post-randomisation
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Liddy Goyder, MD FFPH, University of Sheffield
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Goyder, Elizabeth, et al.
- Copeland RJ, Horspool K, Humphreys L, Scott E; Booster trial team. Recruiting to a large-scale physical activity randomised controlled trial - experiences with the gift of hindsight. Trials. 2016 Feb 24;17(1):104. doi: 10.1186/s13063-016-1229-0.
- Goyder E, Hind D, Breckon J, Dimairo M, Minton J, Everson-Hock E, Read S, Copeland R, Crank H, Horspool K, Humphreys L, Hutchison A, Kesterton S, Latimer N, Scott E, Swaile P, Walters SJ, Wood R, Collins K, Cooper C. A randomised controlled trial and cost-effectiveness evaluation of 'booster' interventions to sustain increases in physical activity in middle-aged adults in deprived urban neighbourhoods. Health Technol Assess. 2014 Feb;18(13):1-210. doi: 10.3310/hta18130.
- Hind D, Scott EJ, Copeland R, Breckon JD, Crank H, Walters SJ, Brazier JE, Nicholl J, Cooper C, Goyder E. A randomised controlled trial and cost-effectiveness evaluation of "booster" interventions to sustain increases in physical activity in middle-aged adults in deprived urban neighbourhoods. BMC Public Health. 2010 Jan 4;10:3. doi: 10.1186/1471-2458-10-3.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
November 1, 2009
Primary Completion (Actual)
December 1, 2012
Study Completion (Actual)
December 1, 2013
Study Registration Dates
First Submitted
February 3, 2009
First Submitted That Met QC Criteria
February 3, 2009
First Posted (Estimate)
February 4, 2009
Study Record Updates
Last Update Posted (Estimate)
December 2, 2014
Last Update Submitted That Met QC Criteria
December 1, 2014
Last Verified
December 1, 2014
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 120243
- HTA: 07/25/02
- IRAS: 08/H1308/270
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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