General Practice, Physical Activity, Primary Care
Conditions
Brief summary
A two-arm parallel randomised controlled trial comparing pedometer-based intervention with and without email counselling in a primary care setting. Physically inactive patients from four general practices will be randomised to the pedometer-plus-email group or to the pedometer-alone group. All patients will be instructed to gradually increase the daily number of steps to at least 10,000. Patients in the pedometer-plus-email group will receive 8 counselling emails based on behavioural techniques. The primary outcome will be change in average daily steps measured during 7-day period at baseline and at 12 weeks.
Interventions
BEHAVIORALpedometer-plus-email
After randomisation, participants will receive a pedometer and will be instructed to wear the pedometer daily for the next four months, check the step count every evening and gradually increase their daily number of steps to at least 10,000. They will also be required to upload data to a website at least once a week. During the intervention period, patients will receive 8 counselling emails based on behavioural techniques.
BEHAVIORALpedometer-only
After randomisation, participants will receive a pedometer and will be instructed to wear the pedometer daily for the next four months, check the step count every evening and gradually increase their daily number of steps to at least 10,000. They will also be required to upload data to a website at least once a week. There will be no further interaction during the intervention period unless they fail to upload data, in which case they will be offered technical support.
Sponsors
Charles University, Czech Republic
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
* physically inactive, i.e. takes less than 8,000 steps per day at baseline * registered at the participating general practice, * over 18 years of age, * regular email user, and willing to use email for the purpose of the study, * has a home computer with access to the Internet.
Exclusion criteria
* medical or psychiatric condition which the general practitioner considers as inappropriate for participating in the intervention (e.g., terminal illness, psychotic illness, chronic disorders or diseases that seriously influence the ability to be physically active, dementia or significant cognitive impairment, unable to move about independently), * medical, personal of family condition which the general practitioner considers temporarily affects mean daily step count at baseline (e.g., acute illness, holiday or business trip), * pregnant woman, * currently engaging in regular sports or exercise (at least twice a week), * failure to upload pedometer data to a website at baseline assessment, * failure to give informed consent with the study.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| average daily step count | 12 weeks | change in average daily steps measured during 7-day period at baseline and at 12 weeks |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| systolic blood pressure | 12 weeks | measured to the nearest mmHg |
| body weight | 12 weeks | measured to the nearest kg |
| diastolic blood pressure | 12 weeks | measured to the nearest mmHg |
| waist circumference | 12 weeks | recorded with a measurement tape to the nearest cm |
| hip circumference | 12 weeks | recorded with a measurement tape to the nearest cm |
Other
| Measure | Time frame | Description |
|---|---|---|
| depression | 12 weeks | assessed with the depression subscale of the Hospital Anxiety and Depression Scale |
| self-efficacy | 12 weeks | assessed with the Czech version of the General Self-Efficacy scale |
| anxiety | 12 weeks | assessed with the anxiety subscale of the Hospital Anxiety and Depression Scale |
| health-related quality of life | 12 weeks | assessed with the 36-Item Short Form Health Survey (SF-36) |
Outcome results
None listed