Skip to content

The use of PRICE (Protection, Rest, Ice, Compression and Elevation) in the management of acute soft tissue injury

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN13903946
Enrollment
106
Registered
2007-02-14
Start date
2007-09-01
Completion date
Unknown
Last updated
2015-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Subjects with acute ankle sprains will be recruited Musculoskeletal Diseases Sprains

Interventions

Group one: Intermittent ice only (10 minutes ice/10 minutes rest /10 minutes ice). Group two: Intermittent ice (10 minutes ice/10 minutes rest /10 minutes ice) plus early mobilisation (patients will b

Sponsors

University of Ulster, Jordanstown (UK)
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Subjects with an acute (less than 72 hours) grade one or two acute ankle injury, between 16 and 65 years of age will be considered for inclusion in the study.

Exclusion criteria

Exclusion criteria: They will not be admitted to the study if any of the following criteria are present: 1. Non English speaking 2. Learning disabilities or mental illness 3. Under the influence of drugs or alcohol 4. A bony ankle injury (diagnosed by Ottawa ankle rules or X-Ray) or ankle ligament rupture 5. Multiple injuries 6. Injuries more than 72 hours old 7. Insufficient address for follow up 8. Unwillingness to return for follow up 9. Contraindication for cryotherapy

Design outcomes

Primary

MeasureTime frame
The primary outcome measure will be subjective ankle function, assessed using Binkley?s lower extremity functional scale. This scale has excellent test retest reliability, and good construct validity. This will be recorded at baseline, one, two, three, four and six weeks post injury.

Secondary

MeasureTime frame
Current secondary outcome measures as of 10/12/2007: 1. Ultrasound imaging of the injured ankle. Subjective and objective measurement of swelling, ligament damage. This will be recorded at baseline, one, two, three, four and six weeks post injury 2. Pain at rest and on activity will be assessed using a 10 cm visual analogue scale 3. Swelling will be measured using a figure of eight method. All measurements will be undertaken using one-quarter inch wide plastic tape following a standard written protocol and valid tool for measuring the girth, of both healthy and oedematous ankles. This will be recorded at baseline, one, two, three, four and six weeks post injury 4. Muscle strength measured on the KinCom 500H Isokinetic Dynamometer, according to a standard written protocol. This will be measured at twelve weeks post injury Previous secondary outcome measures: 1. Ultrasound imaging of the injured ankle. Subjective and objective measurement of swelling, ligament damage. This will be recorded at baseline, one, two, three, four and six weeks post injury 2. Pain at rest and on activity will be assessed using a 10 cm visual analogue scale 3. Swelling will be measured using a figure of eight method. All measurements will be undertaken using one-quarter inch wide plastic tape following a standard written protocol and valid tool for measuring the girth, of both healthy and oedematous ankles. This will be recorded at baseline, one, two, three, four and six weeks post injury 4. Eversion strength will be measured on the Biodex 3 dynamometer, according to a standard written protocol. This will be measured at six weeks post injury

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Apr 6, 2026