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KT Tape for Pediatric Clavicle Fractures

KT Tape vs Arm Sling for Pediatric Clavicle Fractures

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04161534
Enrollment
50
Registered
2019-11-13
Start date
2020-10-01
Completion date
2026-10-01
Last updated
2026-04-02

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

Conditions

Clavicle Fracture

Keywords

arm sling, Kinesiology tape

Brief summary

Clavicle fractures in children are mostly managed non-operatively since they have an overall high union rate (95%) and a "good" functional outcome following nonoperative treatment. However, the downside of such a conservative approach is that patients have to live with pain and disability until the fracture heals. To minimize this, fractures are usually immobilized with a sling. There have been no studies looking at clavicle fractures treated with kinesiology (elastic) tape. No adverse effects (skin irritation, redness, etc.) are observed with the application of this tape. Elastic tape has previously been examined regarding muscular advantages rather than for healing fractures. Since this tape should immobilize fractures better than a sling, patients should experience less pain and disability associated with their fracture.

Interventions

DEVICEKT Tape

in addition to an arm sling, KT Tape will be applied to stabilize the clavicle fracture, thereby decreasing motion and pain.

DEVICEArm Sling

An arm sling will be applied to stabilize the clavicle fracture, thereby decreasing motion and pain.

Sponsors

University of Alabama at Birmingham
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

Participants will be treated with an arm sling and will be randomized to kinesio tape (KT Tape) or no kinesio tape (control)

Eligibility

Sex/Gender
ALL
Age
7 Years to 17 Years
Healthy volunteers
No

Inclusion criteria

* Clavicle Fracture * Injury date within 1 week of presentation

Exclusion criteria

* Underlying neuromuscular disorder (eg osteogenesis imperfecta) * Inability or unwillingness to report pain score until healing

Design outcomes

Primary

MeasureTime frameDescription
Change in Pain ScoreTwice daily for 3 weeks, and one additional time 6 weeks after the initial injnuryParticipants will rate their pain on a scale from 1 to 10

Secondary

MeasureTime frameDescription
Change in Answers to DASH QuestionnaireOnce weekly for 3 weeks, followed by one additional time 6 weeks after the initial injury.Participants will complete the DASH questionnaire to assess disability they might be experiencing due to their fracture.
Change in Analgesic UseOnce daily for 3 weeks, and one additional time 6 weeks after the initial injnuryParticipants will provide the need for taking analgesics (name, dose, and frequency).

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORShawn R Gilbert, MD

University of Alabama at Birmingham

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 3, 2026