Exploring Accessible Beauty for Individuals With Upper Extremity Deficits

Status Completed

Clinical Trial Summary

The purpose of this study is to investigate the accessibility of beauty products for individuals with upper extremity disabilities. By examining various factors such as packaging design, product applicators, and ease of use, this research aims to identify barriers faced by individuals with upper extremity disabilities or visual deficits when using beauty products. The study seeks to provide insights and recommendations for improving the accessibility of beauty products, ultimately promoting inclusivity and enhancing the overall beauty experience for individuals with disabilities.

Clinical Trial Description

Individuals with upper extremity disabilities face unique challenges when it comes to using beauty products. These disabilities can include conditions such as limb loss, limited mobility, or dexterity impairments, which can significantly impact their ability to engage in self-care and beauty routines. The accessibility of beauty products is crucial to ensure that individuals with upper extremity disabilities have equal opportunities to participate in activities that promote self-expression and confidence. Research in the field of accessible design has highlighted the importance of inclusive product development across various industries, including cosmetics and personal care. However, limited attention has been given specifically to beauty products and their usability for individuals with upper extremity disabilities. To address this gap, studies are being conducted to assess the accessibility of beauty products and identify potential barriers and solutions. These studies typically examine factors such as packaging design, ergonomics of product applicators, ease of grip, and maneuverability. By understanding the specific challenges faced by individuals with upper extremity disabilities, researchers can propose modifications and design considerations that enhance accessibility. ;

Study Design

Related Conditions & MeSH terms

Amyotrophic Lateral Sclerosis
Brain Injuries
Brain Injuries, Traumatic
Ehlers-Danlos Syndrome
Graves Disease
Guillain-Barre Syndrome
Hemorrhagic Stroke
Ischemic Stroke
Lupus Erythematosus
Motor Neuron Disease
Multiple Sclerosis
Muscular Dystrophies
Myasthenia Gravis
SCI - Spinal Cord Injury
Sclerosis
Spinal Cord Injuries
Stroke
Stroke (CVA) or TIA
Stroke Hemorrhagic
Stroke, Acute
Stroke, Ischemic
Syndrome
Traumatic Brain Injury
Wounds and Injuries

Clinical Trial Details

NCT number	NCT05945784
Study type	Observational
Source	Casa Colina Hospital and Centers for Healthcare
Contact
Status	Completed
Phase
Start date	July 21, 2023
Completion date	September 29, 2023

View Details

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Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.