"Step by Step": promoting lunchtime walking to increase physical activity and improve mental well-being in sedentary employees

ISRCTN ISRCTN81504663
DOI https://doi.org/10.1186/ISRCTN81504663
ClinicalTrials.gov number NCT01150084
Secondary identifying numbers TBF-08-004
Submission date
25/06/2010
Registration date
10/08/2010
Last edited
29/08/2018
Recruitment status
No longer recruiting
Overall study status
Completed
Condition category
Other
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data

Plain English summary of protocol

Not provided at time of registration

Study website

Contact information

Dr Cecilie Thogersen-Ntoumani
Scientific

School of Sport and Exercise Sciences
College of Life and Environmental Sciences
University of Birmingham
Edgbaston
Birmingham
B15 2TT
United Kingdom

Study information

Study designRandomised waiting list controlled feasibility study
Primary study designInterventional
Secondary study designRandomised controlled trial
Study setting(s)Other
Study typeQuality of life
Participant information sheet Can be found on http://www.bhamstep.co.uk
Scientific title"Step by Step": a feasibility study of the promotion of lunchtime walking to increase physical activity and improve mental well-being in sedentary employees
Study acronymStep by Step
Study objectivesTo examine the feasibility of a sixteen-week lunchtime walking intervention designed to
1. Promote regular walking, and
2. Improve psycho-social well-being and work performance in sedentary employees
Ethics approval(s)University of Birmingham Life and Health Sciences Ethical Review Committee approved on the 31st March 2009 (ref: ERN_09-154)
Health condition(s) or problem(s) studiedPhysical inactivity/sedentary lifestyles
InterventionA sixteen week randomised controlled trial, in which eligible participants will be randomised to an intervention and a waiting-list control group (to start at 10 weeks). The intervention will consist of a group support phase (weeks 1 - 10) and an independence phase (weeks 11 - 16). During the group-support phase, the participants will be asked to join in three weekly lunchtime walks of thirty minutes duration in a facilitator-led group (maximum of 12 per group), and will be challenged to accumulate 60 minutes of walking during the weekend. This would meet national recommendations of 150 minutes/week. The participants will be prompted to add their daily step count in log books at the end of every day. They will also receive two autonomy-supportive messages via a provided smartphone (used for monitoring and motivational purposes) per week during the group phase.

During the independence phase, the group walks will cease to exist on a formal basis, and the participants will be encouraged to engage in a minimum of three weekly lunchtime walks plus two in the week-ends. Formation of smaller informal groups will be recommended. Three weekly autonomy-supportive messages will be provided.
Intervention typeOther
Primary outcome measure1. Step counts: measured daily (week 1 - 16)
2. Numbers of walks attended: measured weekly (week 1 - 10)
Secondary outcome measures1. Job affect
2. Momentary job satisfaction: measured twice per day on two days per week (weeks 1 - 16)
3. Self-reported and manager ratings of work performance: measured at baseline (week 0) and week 17
4. Life satisfaction: measured at week 0, week 17 and 4 month follow-up
5. Subjective vitality: measured at week 0, week 17 and 4 month follow-up
6. Cardiovascular fitness: measured at week 0 and week 17
7. Self-reported levels of physical activity: measured at week 0, week 17 and 4 month follow-up
Overall study start date07/09/2009
Completion date01/03/2011

Eligibility

Participant type(s)Healthy volunteer
Age groupAdult
Lower age limit18 Years
Upper age limit65 Years
SexBoth
Target number of participants68
Key inclusion criteria1. Healthy
2. Mobile
3. Aged 18 - 65 years, either sex
4. Employed in a sedentary job
5. Engaging in less than 30 minutes of moderate intensity physical activity five times per week
Key exclusion criteria1. Significant auditory or visual problems
2. Severe musculoskeletal disorders that prevent them from engaging in physical activity
3. Medical clearance will be requested for those who report any cardiovascular disease
Date of first enrolment07/09/2009
Date of final enrolment01/03/2011

Locations

Countries of recruitment

  • England
  • United Kingdom

Study participating centre

University of Birmingham
Birmingham
B15 2TT
United Kingdom

Sponsor information

University of Birmingham (UK)
University/education

Edgbaston
Birmingham
B15 2TT
England
United Kingdom

Website http://www.bham.ac.uk/
ROR logo "ROR" https://ror.org/03angcq70

Funders

Funder type

Charity

BUPA Foundation (UK)
Private sector organisation / Trusts, charities, foundations (both public and private)
Location
United Kingdom

Results and Publications

Intention to publish date
Individual participant data (IPD) Intention to shareNo
IPD sharing plan summaryNot provided at time of registration
Publication and dissemination planNot provided at time of registration
IPD sharing plan

Study outputs

Output type Details Date created Date added Peer reviewed? Patient-facing?
Protocol article protocol 27/09/2010 Yes No
Results article results 01/12/2015 Yes No

Editorial Notes

29/08/2018: Publication reference added.