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Trial of Arm Sleeve and Forearm Fatigue During Robotic Surgery

Randomized Controlled Trial of Arm Sleeve and Forearm Fatigue During Robotic Surgery

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06860048
Enrollment
32
Registered
2025-03-05
Start date
2023-10-01
Completion date
2024-05-01
Last updated
2025-03-05

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

Conditions

Ergonomics

Brief summary

The study objective was to investigate whether wearing a forearm compression sleeve during robotic surgery reduces muscle fatigue as measured objectively by a grip strength dynamometer.

Interventions

DEVICEArm sleeve

Randomised to wear arm sleeve on left or right

Sponsors

Prince of Wales Hospital, Sydney
Lead SponsorOTHER_GOV

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Robotic surgeon

Exclusion criteria

\-

Design outcomes

Primary

MeasureTime frameDescription
Muscle fatigue2 hours after interventionHand grip strength (muscle fatigue)was assessed at the beginning and at the two-hour mark during the robotic console component of the surgical case, using the Camry Electronic Handgrip Dynamometer (CAMRY model: SCACAM-EH101). The non-sleeve-wearing forearm acted as a control. During testing, the surgeon sat upright with the elbows flexed at right angles by the side of the body and hands in neutral positions (halfway between supination and pronation). The handle was pulled with maximum force for three seconds. The hand grip strength (measured in kg force) was recorded ten times for the dominant (right) and non-dominant (left) hands alternately.

Countries

Australia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026