Eligibility Module

Eligibility Module

The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.

Eligibility Module path is as follows:

Study -> Protocol Section -> Eligibility Module

Eligibility Module


Ignite Creation Date: 2025-12-25 @ 4:50 AM
Ignite Modification Date: 2025-12-25 @ 4:50 AM
NCT ID: NCT04274218
Eligibility Criteria: Inclusion Criteria: Participant inclusion criteria for all participants include: * age between 18 and 65 years * normal or corrected vision * able to walk unassisted for 20 minutes without undue fatigue or health risks Additional inclusion criteria for participants with ULL include: * unilateral ULL at the transradial level * most recent major upper limb amputation occurred at least one year prior to study * residuum and amputated side in good condition (no scars, infections, pain, etc.) * habitual experience using an upper limb prosthesis for at least one year * a self-reported comfortable prosthetic suspension Exclusion Criteria: Exclusion criteria for all participants include: * self-reported additional neurological, vascular, or musculoskeletal pathologies (other than ULL when applicable) that may affect proprioception/balance * self-reported medication that may affect proprioception/balance, e.g.: * drugs that are ototoxic, such as certain Aminoglycosides and pain killers * cognitive deficits that preclude understanding of the study instructions * presence of osteoporosis * presence of pacemakers or stents that may be irritated by the chest harness
Healthy Volunteers: True
Sex: ALL
Minimum Age: 18 Years
Maximum Age: 65 Years
Study: NCT04274218
Study Brief:
Protocol Section: NCT04274218