Isolated blunt chest wall trauma Injury, Occupational Diseases, Poisoning
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Isolated BCWT patient 2. Aged 18 years or more 3. Capacity to consent to participation 4. Capacity to complete survey 5. Length of stay of 24 hours or more
Exclusion criteria
Exclusion criteria: 1. Aged less than 18 years 2. No capacity to consent to participation 3. No capacity to complete survey 4. Length of stay of less than 24 hours
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Recruitment rate recorded as the number of eligible participant who consent to participate in the study by the end of three months 2. Attrition rate recorded as the number of participants who consent to participate that remain in the study until the end of follow up at three months | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Pain measured using the Brief Pain Inventory at baseline and at 3 months post-injury 2. Quality of life measured using the EQ5D-5L at baseline and at 3 months post-injury | — |
Countries
United Kingdom