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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06329934
Other study ID # XXZY-003
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 1, 2022
Est. completion date January 1, 2024

Study information

Verified date May 2022
Source Xinxiang Central Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study is to explore the clinical effect of refined nursing in rehabilitation training for patients with brain injury during the recovery period. Patients in the control group were provided with routine nursing intervention, while patients in the study group adopted a nursing mode based on the concept of refinement treatment. Comparison was made in terms of the Glasgow Coma Scale (GCS) score, cognitive function score, functional independence score, nursing satisfaction, and incidence of complications.


Description:

This study is to explore the clinical effect of refined nursing in rehabilitation training for patients with brain injury during the recovery period. The subjects of the study were 96 patients with severe traumatic brain injury (TBI). According to the order of visits, there were 48 patients in the study group and the control group, respectively.Patients in the control group were provided with routine nursing intervention, while patients in the study group adopted a nursing mode based on the concept of refinement treatment. Comparison was made in terms of the Glasgow Coma Scale (GCS) score, cognitive function score, functional independence score, nursing satisfaction, and incidence of complications.


Recruitment information / eligibility

Status Completed
Enrollment 96
Est. completion date January 1, 2024
Est. primary completion date May 31, 2023
Accepts healthy volunteers No
Gender All
Age group 33 Years to 43 Years
Eligibility Inclusion Criteria: - patients diagnosed with severe TBI through imaging examinations such as head CT and magnetic resonance imaging - patients with surgical indications - patients with Glasgow Coma Scale (GCS) =8 points - patients with complete clinical data - patients with written informed consent provided by family members Exclusion Criteria: - patients with organic lesions of major organs such as liver and kidney - patients with contraindications for surgery - patients with primary diseases such as cerebral hemorrhage and cerebral infarction - patients with combined or multiple injuries - patients with respiratory failure - patients whose family members had cognitive impairment or abnormal mental behaviors

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Establishment of a hierarchical monitoring and management team
To be specific, the head nurse served as the team leader to conduct comprehensive macro supervision; moreover, there were 3 responsible team leaders and 6 responsible nurses, all of whom had rich clinical nursing experience and solid theoretical knowledge of pressure injury. Consequently, a joint-action mechanism of the head nurse - responsible team leader - responsible nurses was developed to facilitate the unification of the training of nursing content, precautions, etc.
Assessment of pressure injury
Based on the postoperative coma of patients, the Braden assessment scale was applied to effectively evaluate patients from six dimensions of sensory perception, moisture, activity mode, mobility, nutrition, friction, and shear. The total score was 23 points. Patients scoring 13~14 points were evaluated by Braden once per week; and those scoring =12 points were evaluated at a frequency of 3d/ time.
Communication
Through intensive face-to-face communication with family members, timely information on the surgical effect, mechanism of pressure injury, preventive measures, and clinical manifestations through intuitive methods such as PPT and video, family members were taught with basic knowledge of pressure injury, and guided to inform medical staff in a timely manner when patients had symptoms of pressure ulcer. Simultaneously, by case sharing and positive suggestions, family members were supported to alleviate their concerns and improve their coordination with treatment
Intervention for pressure ulcer
For patients with a Braden score of >14 points, attention should be paid to keeping skin dry and clean, regularly changing bed sheets and bedding (once per day). Patients with Braden score of 13-14 points should be provided with sponge mattresses, increased times of turning over once per 2 hours, and soft pillows or foam dressings at the site of occipital protuberance to relieve pressure and prevent pressure injury. For patients with Braden score =12 points, medical staff should repeatedly emphasize to their families the harm of pressure injury to postoperative recovery.
Rehabilitation training
After regaining consciousness with stable vital signs, patients received rehabilitation training following the principle of association of activity and inertia in a regular order. Patients were guided to perform upper limb movements, joint flexion, lower limb flexion and extension, as well as daily training such as washing face, rinsing mouth, and dressing at a frequency of 3~4 times/d. Moreover, patients were advised to minimize violent behaviors such as laughing and talking loudly
introduction of the current patient's condition to family members
timely introduction of the current patient's condition to family members to alleviate their concerns
maintaining appropriate temperature and humidity in the ward
maintaining appropriate temperature (20 ?~22 ?) and humidity (60.0%~70.0%) in the ward
careful observation of vital signs in patients
careful observation of vital signs such as heart rate, blood oxygen saturation, and blood pressure in patients

Locations

Country Name City State
China Effect of Refined Nursing in Rehabilitation Training for Patients with Brain Injury During the Recovery Period: An Observational Study Xinxiang Henan

Sponsors (1)

Lead Sponsor Collaborator
Xinxiang Central Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary GCS scores The highest GCS score was 15 points, indicating clear consciousness; while patients with 13-15, 9-12, and =8 points were classified as mild, moderate consciousness disorder, and coma, respectively. Patients with lower scores might indicate more serious consciousness disorder one day before the intervention
Primary GCS scores The highest GCS score was 15 points, indicating clear consciousness; while patients with 13-15, 9-12, and =8 points were classified as mild, moderate consciousness disorder, and coma, respectively. Patients with lower scores might indicate more serious consciousness disorder 2 months after rehabilitation treatment
Primary cognitive function scores Cognitive function was evaluated using the Chinese version of the Neurobehavioral Cognitive Status Exam (NCSE) to assess the cognitive function of patients before and 2 months after rehabilitation treatment. This scale includes 10 items, i.e., spatial orientation (12 points), concentration (8 points), understandability (6 points), retelling (12 points), naming (8 points), spatial construction (6 points), memory (12 points), computing (4 points), similarity (8 points), and judgment (6 points) one day before the intervention
Primary cognitive function scores Cognitive function was evaluated using the Chinese version of the Neurobehavioral Cognitive Status Exam (NCSE) to assess the cognitive function of patients before and 2 months after rehabilitation treatment. This scale includes 10 items, i.e., spatial orientation (12 points), concentration (8 points), understandability (6 points), retelling (12 points), naming (8 points), spatial construction (6 points), memory (12 points), computing (4 points), similarity (8 points), and judgment (6 points) 2 months after rehabilitation treatment
Primary functional independence scores Functional Independence Measure (FIM), utilizing a 7-point ordinal scale, was employed to assess the functional independence of two groups of patients before and 2 months after rehabilitation treatment. FIM measures independent performance in self-care, sphincter control, mobility, locomotion, communication, social cognition, etc. The minimum score is 18 points, and the maximum score is 126 points (91 points for motor function and 35 points for cognitive function) one day before the intervention
Primary functional independence scores Functional Independence Measure (FIM), utilizing a 7-point ordinal scale, was employed to assess the functional independence of two groups of patients before and 2 months after rehabilitation treatment. FIM measures independent performance in self-care, sphincter control, mobility, locomotion, communication, social cognition, etc. The minimum score is 18 points, and the maximum score is 126 points (91 points for motor function and 35 points for cognitive function) 2 months after rehabilitation treatment
Primary Newcastle Satisfaction with Nursing Scale (NSNS) The Newcastle Satisfaction with Nursing Scale (NSNS) was used to survey patient's nursing satisfaction. This scale measures patient's satisfaction with nursing care from 19 items, including nurse work ability, communication attitude, psychological counseling, nursing support, safety management, etc. It uses a 1-5 point scoring system, with a maximum possible score of 19-95 points. A score of =77, 58~76, 39~57 and =38 points indicated very satisfied, satisfied, somewhat satisfied, and dissatisfied, respectively. Satisfaction rate= (Cases of very satisfied + satisfied + somewhat satisfied)÷total cases one day before the intervention
Primary Newcastle Satisfaction with Nursing Scale (NSNS) The Newcastle Satisfaction with Nursing Scale (NSNS) was used to survey patient's nursing satisfaction. This scale measures patient's satisfaction with nursing care from 19 items, including nurse work ability, communication attitude, psychological counseling, nursing support, safety management, etc. It uses a 1-5 point scoring system, with a maximum possible score of 19-95 points. A score of =77, 58~76, 39~57 and =38 points indicated very satisfied, satisfied, somewhat satisfied, and dissatisfied, respectively. Satisfaction rate= (Cases of very satisfied + satisfied + somewhat satisfied)÷total cases 2 months after rehabilitation treatment
Primary incidence of adverse reactions Incidence (%)=Number of patients with complications/48×100% one day before the intervention
Primary incidence of adverse reactions Incidence (%)=Number of patients with complications/48×100% 2 months after rehabilitation treatment
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