Effect of Early Cognitive Stimulation Interventions on Delirium and Cognitive Functions Among Critically Ill Patients

Sponsor
Damanhour University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06115863
Collaborator
(none)
130
2
12

Study Details

Study Description

Brief Summary

Delirium is an acute change in attention and awareness that develops over a relatively short time interval and associated with additional cognitive deficits such as memory deficit, disorientation, or perceptual disturbances.

Delirium negative impact has been widely documented in the medical literature. It has been associated with increased mortality and morbidity, longer hospital stays, increase health care costs, and a longer duration of MV.

Delirium in the ICU can be prevented and treated with a combination of pharmaceutical and non-pharmaceutical interventions.

Cognitive interventions, as part of a delirium prevention strategy, are specific therapies focusing on the domains of cognitive functioning impacted by delirium such as orientation, attention, registration, recall and language.

Cognitive stimulation interventions such as orienting patients to the date, time and place, visual and auditory stimulations that focused on specific domains (orientation and registration). In addition, cognitive stimulation included cognitive training and stimulation exercises that focus on specific domains (attention, language, recall, and registration) such as analyzing exercise, recalling exercise, and cognitive-training exercises by using mobile applications .

The involvement of family members in the cognitive stimulation of critically ill patients is an underutilized resource that may benefit patients as well as gain a sense of control and purpose.

Condition or Disease Intervention/Treatment Phase
  • Other: Early Cognitive Stimulation Interventions
N/A

Detailed Description

Nurses have direct contact with patients 24 hours a day, so they are in an ideal position to prevent, detect, manage, and care for patients who have delirium. The identification of predisposing or precipitating variables must be a part of the nursing intervention in order to reduce the likelihood of delirium occurring. When possible, nurses can help identify at-risk individuals and lower risk. Although a regular nursing assessment and good observational skills combined with a strong therapeutic relationship can enable nurses to recognize sudden changes in attention or consciousness, which are typical indications of delirium.

Although the effects of cognitive stimulation interventions have been extensively studied in the prevention of delirium for ICU patients, there are few studies have implemented to assess its effects when it is applied early within the first 24 hours from ICU admission worldwide, and up to our knowledge there are no national studies that have been conducted to assess early effects of such interventions on delirium in ICU. Therefore, this study will be conducted to evaluate the effect of early cognitive stimulation interventions on delirium in critically ill patients.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
130 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
A randomized controlled trial with two parallel groups will be used in the current study.A randomized controlled trial with two parallel groups will be used in the current study.
Masking:
Triple (Participant, Care Provider, Investigator)
Primary Purpose:
Prevention
Official Title:
Effect of Early Cognitive Stimulation Interventions on Delirium and Cognitive Functions Among Critically Ill Patients
Anticipated Study Start Date :
Nov 1, 2023
Anticipated Primary Completion Date :
Apr 1, 2024
Anticipated Study Completion Date :
Nov 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: placebo group

Delirium and cognitive functions will be assessed for patients in the control group twice per day for five consecutive days' pre and post conventional nursing care. The researcher will observe the conventional nursing care provided by CCNs in the study setting which may affect delirium incidence and patients' cognitive functions for 45 minutes twice daily for five consecutive days. These traditional nursing practices may include a close conversation between the nurse and the patient, patient re-orientation, such as providing information about time, date, and location, tactile stimulation during various procedures, and changing patients' positions.

Other: Early Cognitive Stimulation Interventions
early cognitive stimulation interventions refer to multi-dimensions of stimulative evidenced-based interventions, which are done during the first 24 hours from patient admission to the ICU. They are designed to stimulate cognitive function domains that are impacted by delirium such as attention, registration, recall, and language.

Experimental: early cognitive stimulation Interventions group

Beginning on the first day of the patient's admission to the ICU, the early cognitive stimulation interventions will be implemented for nearly 45 minutes twice daily for five days. One session will be conducted during the morning shift and the other during the evening shift. Each session will include the following: Cognitive stimulation activities will be administered to patients in the intervention group by a member of his family for 15 minutes twice a day for five consecutive days. Cognitive training exercises: The researcher will carry out these exercises for a total of 300 minutes over the course of five days, splitting the time between 30 minutes in the morning shift and 30 minutes in the evening shift.

Other: Early Cognitive Stimulation Interventions
early cognitive stimulation interventions refer to multi-dimensions of stimulative evidenced-based interventions, which are done during the first 24 hours from patient admission to the ICU. They are designed to stimulate cognitive function domains that are impacted by delirium such as attention, registration, recall, and language.

Outcome Measures

Primary Outcome Measures

  1. 1. To assess the effect of early cognitive stimulation interventions on incidence of delirium among 65 critically ill patients by use CAM -ICU. [5 day from patients' admission to ICU.]

    Critically ill patients who undergo early cognitive stimulation interventions have a significantly lower risk of incidence delirium than those who do not. Delirium will be assessed for patients by use the Confusion Assessment Method for the ICU (CAM-ICU).

  2. 2. To investigate the effect of early cognitive stimulation interventions on concentration of cognitive function among 65 critically ill patients. [5 days from patients' admission to ICU.]

    Critically ill patients who undergo early cognitive stimulation interventions show improved cognitive abilities compared to those who do not. the measurement tool for cognitive function is Johns Hopkins Adapted Cognitive Exam

Secondary Outcome Measures

  1. 1. To investigate the effect of early cognitive stimulation interventions on patient's length of ICU stay. [immediately after the intervention.]

    Critically ill patients who undergo early cognitive stimulation interventions have a significantly shorter length of ICU stay than those who do not.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Aged ≥18 years.

  • Newly admitted patients not more than 24 hours.

  • Patient's Richmond Agitation Sedation Scale (RASS) from -1 to +1.

Exclusion Criteria:
  • Patient with pre-existing brain injury and cognitive impairment.

  • Patient who is delirious on admission positive for Confusion Assessment Method for the ICU (CAM ICU).

  • Patient with hearing and visual impairment.

  • Patients who is Hemodynamically unstable.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Damanhour University

Investigators

  • Study Director: Sahar Younes Othman Ramadan, ASS-PROF, Damanhour University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Damanhour University
ClinicalTrials.gov Identifier:
NCT06115863
Other Study ID Numbers:
  • prevention of delirium in ICU
First Posted:
Nov 3, 2023
Last Update Posted:
Nov 3, 2023
Last Verified:
Sep 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Damanhour University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 3, 2023