N/A
N=100
Associated Joint Pain With Controlled Ankle Movement (CAM) Walker Boot Wear
Pain · Ankle Injuries
Bottom Line
View on ClinicalTrials.gov: NCT03312933 ↗Enrolled (actual)
100
Serious AEs
0.0%
Results posted
Jan 2019
Primary outcome: Primary: The Presence and Severity of Secondary Site Pain — 31 Participants
Study Design & Population
- Study type
- Observational
- Phase
- N/A
- Interventions
- —
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Brigham and Women's Hospital
- Primary completion
- Mar 2016
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY The Presence and Severity of Secondary Site Pain |
31 | — |
Summary
This study evaluates the location, frequency and duration of secondary site pain relating to immobilization in a CAM walker boot.
Eligibility Criteria
Inclusion Criteria
- All patients enrolled in the study must have an injury that requires wear of a CAM walking boot for at least two weeks and have ambulation ad libitum without other aids (e.g crutches, canes, scooters, wheelchairs, etc.).
Exclusion Criteria
- Patients will be excluded from the study if they are a recent post-operative patient for lower extremity injury, have an additional acute injury to a lower extremity or back other than the foot or ankle injury being treated by the CAM walking boot at the time of initiation of treatment, have an ongoing or history of lower extremity joint injury, arthritis, or back pain or have restricted weightbearing as instructed by a physician (i.e. for ankle fracture that cannot weightbear).
Data sourced from ClinicalTrials.gov (NCT03312933). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.