Skip to content

Sheffield Physical Activity Booster Trial

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.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00836459
Acronym
Booster
Enrollment
282
Registered
2009-02-04
Start date
2009-11-30
Completion date
2013-12-31
Last updated
2014-12-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Public Health

Keywords

Humans, Middle Aged, Behavior Therapy, Directive Counseling, Health Behavior, Interview, Psychological, Motivation, Exercise, Physical Fitness, Self Efficacy, Life Style, Health Promotion, Health Knowledge, Attitudes, Practice, Body Mass Index, Monitoring, Ambulatory, Walking

Brief summary

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.

Interventions

BEHAVIORALMini Booster

Two telephone-based physical activity consultations, delivered in a motivational interviewing style, at one month and two months from randomisation

BEHAVIORALFull Booster

Two face-to-face physical activity consultations, delivered in a motivational interviewing style, at one month and two months from randomisation

Sponsors

NHS Health Technology Assessment Programme
CollaboratorOTHER
Richard Hudson
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
40 Years to 64 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frame
Physical activity measured by accelerometry.3 months post-randomisation

Secondary

MeasureTime frame
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 week3 months and 9 months post-randomisation
Health-related quality of life using the Sheffield Version SF-12v2 plus 4 survey instrument3 months and 9 months post-randomisation
Physical activity assessed by accelerometry.9 months post-randomisation
Self-reported health and social care contacts3 months and 9 months post-randomisation
Psychological measures of motivation, assessed using BREQ-2 (Mullan et al, 1997)3 months and 9 months post-randomisation
Self-reported use of community facilities for physical activity3 months and 9 months post-randomisation

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 1, 2026