Musculoskeletal Diseases or Conditions Clinical Trial
Official title:
Validation and Implementation of a Digital Assessment Routing Tool (DART) as an Alternative to Physiotherapy-led Remote Triage for Musculoskeletal Disorders: Protocol for a Pilot Randomised Crossover Non-inferiority Trial
Verified date | May 2021 |
Source | Queen Mary University of London |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
In the pilot study, we aim to explore trial design, assess procedures, and collect exploratory data to inform the design of a future Randomised Controlled Trial. The intervention involves a Digital Assessment Routing Tool (DART) that provides triage outcomes with recommended management pathways for participants with musculoskeletal problems. Participants complete DART either before or after their consultation with usual care clinicians (Physiotherapy-led remote triage). The triage outcome dispositions between DART and usual care clinicians will be compared. A panel will be formed to provide consensus on disagreements that may result in adverse triage outcomes, as well as on a sample of agreements between DART and usual care clinicians.
Status | Completed |
Enrollment | 78 |
Est. completion date | July 25, 2022 |
Est. primary completion date | July 25, 2022 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - A current musculoskeletal injury for which they are seeking treatment - Over 18 years old - Able to read and speak English - Live in the UK - Able to access the internet Exclusion Criteria: - Cognitive impairments or learning disabilities that limits the participants to follow study- related procedures - Unwillingness or inability to follow protocol-related procedures - Optima Health employees - Has an assessment from a health care professional for the same condition within the last 7 days |
Country | Name | City | State |
---|---|---|---|
United Kingdom | Haydock Medical Centre | St Helens | Herts |
Lead Sponsor | Collaborator |
---|---|
Queen Mary University of London | Optima Health |
United Kingdom,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Proportion of participants identified, shown interest to participate, and recruited to the study. | Participants drop-out rates at each stage of the trial (and where possible reasons for dropping out) will be collected. A pre-defined criterion of 50% and 95% will be considered satisfactory for the proportion of identified participants recruited and retained, respectively. | Through study completion, an average of 3 months. | |
Other | The number of errors reported in randomisation, allocation concealment, blinding or data collection. | System process outcomes include errors reported in randomisation, allocation concealment, blinding or data collection. Any evidence for selection bias or other sources of bias will be explored. | Immediately after the intervention. | |
Other | Time burden (in minutes) of interventions. | The overall time burden (in minutes) will be estimated from initial participant contact to first treatment, along with any treatment delay due to the additional time required to perform research procedures. | Immediately after the intervention. | |
Primary | The agreement rate between triage outcomes with management pathways from physiotherapy-led and DART triage assessments. | The primary outcome measure will be the agreement rate of triage decisions made by both the clinician and the Digital Assessment Routing Tool (DART). The possible triage outcomes with management pathways are classified in three categories, namely 1) Medical care, 2) Physiotherapy care, and 3) Self-management.
Medical care A&E referral Urgent GP Routine GP Consultant review Physiotherapy care Post-fracture or surgery physiotherapy Physiotherapy referral Physiotherapy referral plus psychosocial support Self-management Self-management Self-management with SOS Continue self-management advice |
Immediately after the intervention. |
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