The Relationship Between Lost Extremity Percentage and Postural Control, Neck and Low Back Pain, Daily Living Activities, and Reaction Time in Individuals With Unilateral Upper Limb Amputation

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-65
SponsorHacettepe University

About this trial

This observational study aims to examine the relationship between the percentage of limb loss and functional outcomes in individuals with unilateral upper limb amputation. Upper limb amputation can affect posture, balance control, pain levels, daily living activities, hand function, and reaction time. However, limited research has investigated how the amount of limb loss influences these outcomes.

Participants between 18 and 65 years of age who use a myoelectric or bionic prosthesis will undergo a series of assessments. These assessments include measurements of postural control using a force platform, posture analysis, evaluation of neck and low back pain using a visual analog scale, daily living activities using a validated questionnaire, hand dexterity using the Box and Block Test, and reaction time using a visual stimulus device.

The study does not involve any intervention or treatment. All evaluations will be performed during a single assessment session. The results of this study may help improve rehabilitation planning and provide better understanding of functional changes associated with different levels of limb loss in people with upper limb amputation.

Eligibility criteria

Qualifiers

Adults aged 18-65 years

Unilateral upper limb amputation

Use of a myoelectric or bionic prosthesis for at least 1 year

Current prosthesis use for a minimum of 3 months

Disqualifiers

Bilateral upper limb amputation

Additional amputation of another limb

Use of passive or cosmetic prosthesis

Presence of neurological or other significant orthopedic disorders unrelated to amputation

Trial design

Treatments tested in this trial

  • This is an observational study. No interventional procedures are performed. All assessments are non-invasive measurements.

Treatment groups

15 Participants
are divided into 1 treatment group

Sponsors and collaborators