Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
20969 participants
OBSERVATIONAL
2021-11-26
2022-04-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Which Automated Methodology?
NCT06049056
Feasibility of Care Coordination
NCT04171596
Learning and Relationships in Primary Care
NCT00657696
CHW Intervention to Improve Nutrition Security of Patients With Hypertension
NCT06358417
Enhanced Care for Patients With Complex Multimorbidity in Primary Care
NCT05676541
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Keele Clinical Trials Unit (CTU) quickly implemented online data collection methodologies during 2020, in order to continue with recruitment of and retention of research participants and in response to the national lockdown and tiered systems implemented for protection of the population during the pandemic. There is now opportunity, to re-evaluate the proportion of primary care patients that would be happy to be contacted about research of relevance and also to assess the utility of online technologies, in particular SMS text messaging and an online survey platform, in the collection of the research data.
The specific research objectives of this study are:
1. To examine patient response rates to an invitation to complete an online Keele Health Survey questionnaire, delivered by SMS message from their general practice,
2. To examine the difference in patient response rates to the invitation to participate in the research study with and without a precursor test message (SMS).
3. To estimate the number of patients that would be happy to be contacted about future research studies relevant to their health.
4. To explore any demographic variances in completion responses.
5. To estimate research question completion rate feasibility, for future use of SMS messages containing a link URL to an online Keele Health Survey questionnaire to collect research data.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
ECOLOGIC_OR_COMMUNITY
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Pre-cursor text
A pre-notification text message (SMS) will be sent to eligible people informing them of their imminent invitation to participate in The Who, two days later a brief text message (SMS) will be sent from the general practice to eligible people, inviting them to participate in The Who.
No interventions assigned to this group
Invitation only
A brief text message (SMS) will be sent from the general practice to eligible people, inviting them to participate in The Who.
No interventions assigned to this group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Mobile telephone number must be registered at general practice (doctor's surgery)
Exclusion Criteria
* Anyone who does not have their mobile phone number registered with their general practice (doctor's surgery)
18 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Keele University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Sarah Lawton, MPhil
Role: PRINCIPAL_INVESTIGATOR
Head of Operations - Clinical Trials Unit
Christian Mallen, Professor
Role: STUDY_DIRECTOR
Head of School of Medicine
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Keele University: School of Medicine
Newcastle-under-Lyme, Staffordshire, United Kingdom
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
IRAS Number: 291348
Identifier Type: OTHER
Identifier Source: secondary_id
RG-0322-21
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.