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Access-H20: Sensor-driven Smart Faucet Related Study

19 maggio 2026 aggiornato da: Anna Jeng, Old Dominion University

Access-H20: Sensor-driven Smart Faucet to Enable and Empower Independent Drinking and Grooming for Individuals Impacted by Spinal Cord Injury

The objective of the SBIR Phase II study is to evaluate the updated Access-H2O™ system, a sensor-driven smart faucet developed during the Phase I SBIR project, to enhance independent drinking and grooming among individuals with spinal cord injury (SCI) in both clinical and home settings. SCI significantly impairs functional independence and the ability to perform activities of daily living (ADLs), with greater loss of function associated with higher and more complete injuries. In particular, individuals with injuries above the C5-C7 level often experience substantial upper extremity impairment, limiting their ability to use their arms and hands for essential tasks such as eating, drinking, and grooming. Access to water is therefore critical for supporting independence and facilitating the successful completion of ADLs in this population.

The commercialization of a smart faucet system capable of automatically delivering water at target temperature, flow rate, and nozzle settings tailored to specific ADLs has the potential to substantially improve independence and quality of life for individuals with SCI. The Access-H2O™ faucet was developed and tested during the SBIR Phase I project in 2024 and was subsequently upgraded and refined based on Phase I findings. Participants with SCI, along with control participants, were recruited to evaluate the usability of the enhanced faucet system in both clinical and in-home settings. The updated system incorporates voice, motion, and remote-control interfaces to regulate water flow and temperature for ADLs, including drinking, grooming, and washing.

Panoramica dello studio

Stato

Completato

Intervento / Trattamento

Descrizione dettagliata

Conventionally, a bathroom faucet includes a hot and cold-water knob used to control flow of water through the faucet, which is utilized for hand washing, face washing, rinsing after brushing, etc. However, existing faucets are inconvenient to use for purposes other than conventional hand washing, unhygienic, and result in wasting large amounts of water. Existing faucets make it difficult for individuals with cervical spinal cord injury (SCI) to carry out basic activities of daily living (ADLs), such as drinking, rinsing their mouths, and washing their faces.

To address these challenges, Nasoni Inc. develop the new faucet, Access H2OTM faucet, to address these challenges. During the Phase I study from 2022-2023, the investigators achieved the following objectives: 1) successfully designing and producing a prototype of the Access H2O faucet that met input specifications in bench testing, and 2) developing control algorithms using sensor-based inputs successfully allowed both control and SCI subjects to accurately access desired water. The Phase I study showed that the faucet could improve water access for SCI subjects and improve their ADLs. SCI subjects showed a strong preference for Access-H2O faucets compared to traditional methods.

Before proceeding with commercialization, it is necessary to optimize the operational functions of the prototype. In the Phase II study, the engineering team has enhanced the prototype's faucet form factor design and sensors based on the findings from the Phase I study. These enhancements include: 1) optimizing the form factor and nozzle water delivery, 2) refining the sensor & display components, and 3) expanding sensor integration capabilities. Also, the team has improved the water control mechanisms established in Phase I by integrating Access-H2O faucet intelligent algorithms and developing a supporting digital platform with a mobile app to support product efficacy, usability, and field maintenance.

Specifically, Phase II evaluates improvements in faucet form factor, sensor placement, manufacturing-ready hardware, and interaction modalities, all informed by Phase I user feedback and clinical observations. Accordingly, the objective of this Phase II study is to assess system refinements that impact real-world independence and usability of the refined faucet. The Year 1 testing was conducted in a clinical setting. The specific aims of the clinical assessment were to evaluate the usability of the refined Access-H2O™ faucet system-controlled via voice commands, hand motion, and a wireless remote-to drink water (drinking), rinse the face (grooming), or wash hair (washing; optional). Besides the unique water floor technology, the Access-H2O™ faucet system equips hand-free methods for water access and water temperature control:

  • Voice control via keyword recognition using Alexa integration
  • Motion control using a time-of-flight (ToF) proximity sensor
  • Wireless remote control with tactile buttons (newly introduced in Phase II)
  • Raised spout (+5 cm) and re-angled water stream for seated face washing and hair rinsing
  • Temperature control system using PID logic and a 40°C thermal safety cap There are three control sensors: voice, motion, and remote controls. Voice recognition is enabled through integration with a pre-existing Amazon Alexa device using a custom Alexa Skill. Users activate the system by saying "Alexa" followed by predefined commands (e.g., "Faucet on" or "Turn on Grooming Mode") to control faucet operation, mode selection, and temperature hands-free. Motion detection is implemented using ToF proximity sensors mounted at the base of the faucet to detect hand motion to activate the faucet for water dispensing. A handheld wireless remote control that provides an alternative input method for operating the faucet with maximal flexibility in placement and use. The remote communicates with the faucet via Bluetooth and allows users to activate or deactivate water flow and select among predefined water delivery modes. The remote may be positioned on a nearby surface or affixed using hook-and-loop fasteners, allowing users to locate the control within comfortable reach. On the front of the control, three buttons labeled "F," "W," and "G" correspond to fountain, washing, and grooming, respectively.

In the Year 1 testing, a total of 18 subjects living with SCI, called SCI subjects, and 5 control subjects were recruited in an outpatient rehabilitation clinic. Controls without limitations in head, trunk, or arm movement were used to verify that all faucet functions operated correctly and that water was accessible for drinking, rinsing, and grooming. This preliminary assessment by the controls was conducted after installing the Access-H2OTM faucet in the rehabilitation clinic and before SCI subjects' participation.

The useability testing was conducted to test the faucet's voice, motion, and remote control sensors for SCI subjects' ADLs - drinking, grooming, or washing (optional). We sought answers to the following questions: 1) Can the test participants use voice, motion, and remote controls to activate the faucet to get their mouth to drink/hydrate? 2) Can the test participants use the three controls to rinse a quarter-sized area of soap partially or fully from their left or right cheek or 3) can the test participants use the three controls to wash a quarter soap in hairs.

In the Year 1 testing, all SCI subjects who relied on wheelchairs were seated in their own manual or power wheelchairs. The wheelchairs were positioned in front of a sink equipped with the Access-H2OTM faucet. Sufficient space was provided to accommodate the subjects' legs under the sink, ensuring standardized data collection. Then, the physical therapist who provided scripted instructions to each participant on how to turn on the faucet, and then turn off the faucet. During setup, the system was tested and calibrated to ensure proper operation. If any function did not meet the standard, manual adjustments were made as needed. For example, during setup, flow and spray angles for fountain mode and grooming mode can be customized by adjusting valve angles or water pressure to achieve the preferred water flow trajectory.

Once the system was ready, each SCI subject was asked to place his or her hand by the motion sensor (motion control), use a speech speaker (voice control), and push the remote control to activate water output modes for drinking, grooming, or washing. Each participant performed the same activity (drinking, grooming, or washing) and sensor controls (voice, motion, and remote) three times. For example, a subject used the voice control to activate fountain mode for drinking and repeated the procedure three times. A total of 27 tests were conducted (3 sensors x 3 modes x 3 repetitions). Each activity was recorded "complete," "partially complete," or "unable to complete." The investigators also recorded the time it took for each subject to complete each activity.

Tipo di studio

Interventistico

Iscrizione (Effettivo)

23

Fase

  • Fase 2

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

    • Virginia
      • Norfolk, Virginia, Stati Uniti, 23508
        • Monarch Physical Therapy Clinic

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

Descrizione

Inclusion Criteria:

  • ages 18 to 90 years old
  • screened by a physical or occupational therapist to verify your spinal cord injury (SCI),
  • able to follow instructions,
  • able to move their eyes and head up, down, and right to activate sensors
  • able to safely access a bathroom at home.

Exclusion Criteria:

  • have cognitive deficits, mental health, or medical conditions that would keep them from participating in this study

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Fattibilità del dispositivo
  • Assegnazione: N / A
  • Modello interventistico: Assegnazione di gruppo singolo
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Altro: Faucet Water Output Activation
Arm Description: Year 1 Study (in Clinic): Each subject was instructed to activate the water output modes for drinking and grooming using three different control methods of the faucet: placing their hand near the motion sensor (motion control), using a speech speaker (voice control), and using a remote sensor. For each activity of daily living (drinking and grooming), the physical therapist rated and recorded as "task completed", "partially completed", and "not completed."
Accesso al rubinetto H2OTM è un rubinetto intelligente e senza mano progettato per facilitare l'accesso all'acqua per limitazioni fisiche

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Number of Participants with Water Output Mode Activation
Lasso di tempo: From the start of testing to the completion up to 4 hours
Each subject was measured to determine whether he or she can complete using the Access H2O faucet in clinic for drinking, grooming, and washing. Primary outcomes were recorded as "task completed", "task partially completed", and "not completed" using the Access H2O faucet for drinking, grooming and washing.
From the start of testing to the completion up to 4 hours

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Investigatori

  • Investigatore principale: Anna Jeng, ScD, Old Dominion University

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

1 febbraio 2024

Completamento primario (Effettivo)

31 agosto 2024

Completamento dello studio (Effettivo)

31 agosto 2024

Date di iscrizione allo studio

Primo inviato

27 aprile 2026

Primo inviato che soddisfa i criteri di controllo qualità

19 maggio 2026

Primo Inserito (Effettivo)

22 maggio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

22 maggio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

19 maggio 2026

Ultimo verificato

1 maggio 2026

Maggiori informazioni

Termini relativi a questo studio

Parole chiave

Altri numeri di identificazione dello studio

  • R43HD108061 (Sovvenzione/contratto NIH degli Stati Uniti)
  • 2R44HD108061-02 (Sovvenzione/contratto NIH degli Stati Uniti)

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Descrizione del piano IPD

We don't plan to share individual participant raw data; however, aggregated and tabulated data will be published in peer-reviewed articles.

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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Prove cliniche su Rubinetto d'acqua

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