The Use of Auditory-visual Stimulation to Reduce Delirium Rates in Intensive Care Patients Post-cardiac Surgery: a Feasibility Study

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

STUDY SUMMARY STUDY DESIGN The study will be conducted over twelve months in the Cardiac Intensive Care Unit (ICU) at Hammersmith Hospital, Imperial College Healthcare NHS Trust (ICHT). This study is a mixed methods research design that includes the collection of data through qualitative interviews, quality-of-life questionnaires and patients' medical records. AIMS * Determine the incidence of ICU delirium in ICHT following cardiac surgery * Explore the compliance of outcome measures that diagnose ICU delirium * Implement a family-focused sensory stimulation programme in the ICU * Evaluate its useability and potential impact on patients, families and ICU staff STUDY POPULATION 30 study participants (12 patients, 12 family members/friends and 6 ICU nurses) ELIGIBILITY Study eligibility criteria are specific for each care group (patients, family members/friends and ICU nurses). DURATION 12 months at Hammersmith Hospital, ICHT

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

⁃ Patients

• Female and male patients over the age of 18

• Participants speaking English language and having mental capacity to consent

• Suitable to undergoing cardiac surgery at ICHT.

⁃ Family Members/Friends

• Nominated by the participant.

• Be willing to record videos and participate in the study.

⁃ Healthcare professionals

⁃ \- Critical Care Nurses that have provided direct care to at least one patient who received the study intervention

Locations
Other Locations
United Kingdom
Imperial College Healthcare NHS Trust
RECRUITING
London
Contact Information
Primary
Maria Reguenga, BSN
maria.reguenga@nhs.net
07585095566
Backup
Sanooj Soni, PhD
sanooj.soni@nhs.net
07714329708
Time Frame
Start Date: 2024-03-20
Estimated Completion Date: 2025-03-20
Participants
Target number of participants: 30
Treatments
Experimental: Patient Arm
12 patients will be recruited pre-operatively and submitted to the study intervention
Related Therapeutic Areas
Sponsors
Leads: Imperial College Healthcare NHS Trust

This content was sourced from clinicaltrials.gov