What this study is
The goal of this study is to evaluate whether a voice-activated call light system enables people in a rehabilitation facility who have limited use of their arms and hands to call for help more independently and reliably than with their previous call light access method. The study will also examine client confidence, family confidence and peace of mind, staff confidence, staff effort, system reliability, and the level of disruption to routine care. The main questions to be answered are:
1. People with what etiologies benefit most from access to the voice-activated call light system? 2. How reliable is the voice-activated call light system in alerting staff to a client's need for assistance? 3. How confident are clients, family members, and staff in the reliability of the voice-activated system for alerting staff of a client's need for assistance? 4. How does access to the voice-activated call light system compare to traditional call light systems regarding staff effort and disruption to routine care? Participants with limited upper extremity movement will use the voice-activated call light system as needed during normal daily activities for up to 90 days. At study initiation, clients with limited upper extremity movement, staff members working with those clients, and family members of the clients will complete a brief questionnaire about their experiences using the existing call light system. At approximately Days 30, 60, and 90, they will complete brief questionnaires about use of the voice-activated call light system and its effectiveness.
What's being tested
- voice-activated call light
Intervention · DEVICE
Use of a voice-activated call light will substitute for use of a standard hand-activated call light.
Study details
- Sponsor
- Quality Living, Inc.
- Conditions
- Spinal Cord Injury (=3 Years) · Traumatic Brain Injury (TBI) Patients · Healthy Adult Participants
- Enrolling
- 80 people
- Starts
- 2026-10-15
- Est. completion
- 2027-12-31
- Record
- View on ClinicalTrials.gov ↗
Who can join
Age 19 Years and overSex ALLHealthy volunteers AcceptedYou may qualify if
- Participants with limited upper extremity movement will be current clients at Quality Living, Inc., in Omaha, NE.
- Staff participants will be current employees at Quality Living, Inc., who routinely work with participating clients with upper extremity movement limitations.
- Family member participants will be family members of participating clients with upper extremity movement limitations.
- All participants must be 19 years of age or older.
You can't join if
- Clients with limited upper extremity movement who cannot consistently produce the selected wake phrase due to memory or cognitive difficulties.
- Clients with limited upper extremity movement who have not retained the legal right to make their own healthcare decisions.
Sign in and we'll check these against your records.Full criteria on ClinicalTrials.gov ↗
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Study locations (1)
1 openQuality Living, Inc.
Omaha, Nebraska, United States
Study team
Sponsor
Quality Living, Inc.
Study ID QualityLiving WillCall
Study director
Karen Hux
Quality Living, Inc.
Frequently asked questions
The sponsor hasn't published answers to common questions for this trial.