Communication Barriers

4

Review clinical trials related to Communication Barriers. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Eye-Tracking Communication Tool for Non-verbal ICU Patients

The objectives of this clinical trial are to explore the feasibility of the eye-tracking communication tool in alleviating communication barriers among non-verbal ICU patients. It will also preliminarily investigate the effectiveness of this tool in facilitating communication for these patients. Researchers will compare the eye-tracking communication tool with conventional techniques (such as body language, writing boards, etc.) to observe the feasibility and preliminary effectiveness of the eye-tracking communication tool in alleviating communication barriers. Participants will use an eye-tracking communication tool for augmentative communication for 2 consecutive days.

Participants needed: 40
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Shanghai Zhongshan HospitalUpdated: May 27, 2026
Eligibility criteria

aged ≥ 18 years [+4]

blindness or inability to elevate the eyelids that preclude successful participa... [+2]

Status: Recruiting

Video-Interpreting in Prehospital Emergency Medicine - Feasibility Study

50 responsive patients with language barriers will be included in this study. The prehospital emergency physician will start video-interpreting via a tablet. Feasibility, quality of communication, usability as well as changes in diagnosis and treatment will be gathered and analysed.

Participants needed: 50
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Medical University of ViennaUpdated: Apr 20, 2026Locations: 1
Eligibility criteria

adult patients, at least 18 years old [+2]

unconscious patients [+3]

Status: Not yet recruiting

Eye-Tracking Interactive Agent in Non-verbal ICU Patients

The goal of this clinical trial is to determine whether an eye-tracking interactive agent can ameliorate communication impairments and reduce the incidence of complications among non-verbal patients in the intensive care unit (ICU). The main questions it aims to answer are: Does the eye tracking interactive agent alleviate communication impairments among non-verbal patients in the ICU? Does the eye tracking interactive agent improve communication efficiency among non-verbal patients in the ICU? Does the eye tracking interactive agent m reduce the incidence of negative emotions among non-verbal patients in the ICU? Does the eye tracking interactive agent shorten the ICU length of stay for non-verbal patients in the ICU? Does the eye tracking interactive agent reduce the dosage of analgesic and sedative medications for non-verbal patients in the ICU? Does the eye tracking interactive agent improve family satisfaction for non-verbal patients in the ICU? Does the eye tracking interactive agent alleviate nurses' communication burden among non-verbal patients in the ICU? Researchers will compare eye tracking interactive agent to conventional techniques to see if e eye tracking interactive agent works to alleviate communication impairments. Participants will: Use an eye tracking interactive agent for augmentative communication for 2 consecutive days Document each communication's details, ICU LOS, and analgesic-sedative dosages; assess communication difficulty severity, delirium, anxiety, family satisfaction and nurses' communication burden with validated scales.

Participants needed: 54
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Shanghai Zhongshan HospitalUpdated: Feb 24, 2026
Eligibility criteria

Aged ≥ 18 years [+5]

Diseases associated with cognitive impairment, such as pulmonary encephalopathy,... [+2]

Status: Recruiting

Options for Lowering the Threshold to Brussels Out-of-hours Primary Care Services for Dutch Speaking Citizens

The purpose of this qualitative study is to find out which technological translation tools can be used to improve Dutch-speaking care in all Brussels out-of-hours primary care services.

Participants needed: 40
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Universitair Ziekenhuis BrusselUpdated: Dec 27, 2024Locations: 1
Eligibility criteria

Patients: adult, living in Brussels, Dutch-speaking [+2]

Subject is not capable of will [+1]