- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04556695
Exploration of Sedentary Behaviour Among General Practitioners: A Mixed Methods Study
September 12, 2022 updated by: NeilHeron, Queen's University, Belfast
A sequential, mixed-methods study exploring sedentary behaviour among General Practitioners and General Practice Specialty Trainees.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The study follows a sequential, mixed-methods model involving three stages.
The first stage will involve the dissemination of a questionnaire survey, in which participants will self-estimate their sedentary behaviour on a working day and on a non-working day.
The second stage will involve the use of thigh-worn accelerometers and a sleep/work log to obtain objective data regarding sedentary behaviour among a purposive subset of participants who responded to the questionnaire.
The third stage will involve semi-structured interviews with a purposive subset of participants who wore the accelerometers, which will be analysed with the application of a theoretical framework regarding the acceptability of healthcare interventions.
Study Type
Observational
Enrollment (Actual)
400
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
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Belfast, United Kingdom, BT9 7BL
- Queen's University Belfast School of Medicine, Dentistry and Biomedical Sciences
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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
23 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
General Practice Specialty Trainees (GPSTs) and General Practitioners (GPs) throughout Northern Ireland.
GPs and GPSTs in Northern Ireland provide care for patients as part of the UK NHS, with working conditions similar to GPs and GPSTs throughout the rest of the UK.
Description
Inclusion Criteria:
Participants will be General Practitioners or General Practice Specialty Trainees working in Northern Ireland, United Kingdom.
Exclusion Criteria:
Not working as a General Practitioner or General Practice Specialty Trainee in Northern Ireland, United Kingdom.
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Questionnaire survey
An initial online questionnaire, based on the International Sedentary Assessment Tool (ISAT), will be distributed to General Practice Specialty Trainees (GPSTs) and General Practitioners (GPs) throughout Northern Ireland.
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Online questionnaire, based on the International Sedentary Assessment Tool (ISAT)
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Accelerometer study
A purposive sample of questionnaire respondents will be asked to participate in the accelerometer study.
This purposive sample will be based on responses to the online questionnaire.
The aim will be to obtain a varied sample, based on questionnaire responses, by selecting individuals with a range of demographic characteristics and self-reported levels of sedentary behaviour.
Some participants will also be asked to complete a further online survey, while wearing the accelerometer, regarding their health, wellbeing, burnout and fatigue.
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Online questionnaire, based on the International Sedentary Assessment Tool (ISAT)
Consenting participants will be asked to wear an accelerometer on the lateral aspect of the middle of the right thigh (over the midpoint of the iliotibial band), continuously over a seven-day period.
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Semi-structured interview study
A purposive sample comprising participants of the accelerometer study will be asked to participate in semi-structured interviews.
This purposive sample will be based on the accelerometer data.
The aim will be to obtain a varied sample, based on accelerometer data, by selecting individuals with a range of different levels of sedentary behaviour, demographic and workplace characteristics.
The final number of participants will depend on the saturation of information.
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Online questionnaire, based on the International Sedentary Assessment Tool (ISAT)
Consenting participants will be asked to wear an accelerometer on the lateral aspect of the middle of the right thigh (over the midpoint of the iliotibial band), continuously over a seven-day period.
Semi-structured interviews will take place via telephone or webcam.
Participants will be given feedback regarding their accelerometer data relating to their levels of physical activity and sedentary behaviour.
Questions will examine participants' thoughts and opinions regarding sedentary behaviour and physical activity in the General Practice setting.
Further questions will explore participants' experiences of wearing accelerometers, their knowledge of and attitudes towards physical activity and sedentary behaviour and their thoughts or suggestions on interventions to reduce sedentary behaviour among GPs and GPSTs.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Self-reported sedentary behaviour
Time Frame: Autumn 2020
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Autumn 2020
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Accelerometer measured sedentary behaviour
Time Frame: Autumn 2021
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Autumn 2021
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Thematic analysis of semi-structured interviews
Time Frame: Autumn 2021
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Autumn 2021
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Neil Heron, Centre for Public Health, Queen's University Belfast
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 (Actual)
September 2, 2020
Primary Completion (Actual)
January 1, 2021
Study Completion (Actual)
October 1, 2021
Study Registration Dates
First Submitted
September 14, 2020
First Submitted That Met QC Criteria
September 14, 2020
First Posted (Actual)
September 21, 2020
Study Record Updates
Last Update Posted (Actual)
September 13, 2022
Last Update Submitted That Met QC Criteria
September 12, 2022
Last Verified
September 1, 2022
More Information
Terms related to this study
Other Study ID Numbers
- MHLS 20_39 - Amendment 1
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
Sharing of study protocol to optimise openness and integrity of research.
IPD Sharing Time Frame
Study protocol will be made available on commencement of the study and will be available for the duration of the study.
IPD Sharing Access Criteria
Study protocol will be submitted for open access journal publication.
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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