Casting away burn stiffness: a new hope for arm movement?
NCT ID NCT05425433
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at whether serial casting (applying a cast that is changed weekly) can improve arm and hand movement in adults who have stiff joints from burn scars. Twelve burn survivors with limited range of motion received one week of usual care, then serial casting if needed. Researchers measured joint movement, scar quality, and how well people could use their arm, checking if improvements lasted three weeks after stopping casting.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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12 people
The number who actually took part.
- Started
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Sep 2022
- Finished
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Sep 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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16 to 100 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Burn survivors with \>15% loss of PROM of their PIP, MCP, wrist, or elbow in either: flexion, extension, ulnar deviation or radial deviation. * Fire, flame or scald burn injury -≥16 years old * have provided informed consent. Exclusion Criteria: * Frostbite, chemical or electrical burn injury * A premorbid musculoskeletal or neurological disorder that limited their ROM * Have sustained a neurological injury secondary to the burn injury * A psychiatric or cognitive disorder that limits their ability to follow the research protocol * Have been diagnosed with heterotopic ossification * PROM is contraindicated for any reason * Do not understand English or French.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Hôpital de réadaptation Villa Médica
Montreal, Quebec, H2X 1C9, Canada
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