Delirium in Old Age, Hip Fractures
Conditions
Keywords
delirium, hip fracture, music, randomized controlled trial
Brief summary
The aim of this trial is to explore the efficacy of music in preventing delirium in elderly patients with hip fracture. The main aims of this research are: 1. To compare the effectiveness of music intervention in preventing delirium in patients with hip fractures through a randomized controlled trial. The comparisons include respiratory rate, pulse rate, blood pressure, and pain score, as well as the incidence and severity of delirium, opioid analgesic usage, postoperative complications, length of hospital stay, and rates of readmission within 14 days and 30-day mortality. 2. Introduce the evidence-based ''listening music protocol'' in the care of hip fracture patients to prevent delirium, and test the effects through a randomized controlled trial.
Detailed description
This study is a two-group, pre and post-test, randomized controlled trial to test the effectiveness of the ''listening music protocol''. Convenience sampling will be used to select the inpatients with hip fractures in a regional hospital in southern Taiwan. 102 participants will be randomly assigned either to an experimental (n=51) or to a control (n=51) group. The experimental group will receive a six-day music protocol and regular post-operative care. The control group will receive regular post-operative care only. Statistical analysis was performed using SPSS Version 22.0. Descriptive statistics, including frequencies, percentages, means, and medians, were used to analyze basic attributes. For the analysis of homogeneity, the chi-square test or Fisher's exact test was employed for categorical variables. The paired t-test was used to compare respiratory rate, pulse rate, blood pressure, and pain index. Following the intervention, the occurrence and severity of delirium before and after implementing music intervention were compared. Additionally, comparisons were made for opioid analgesic usage, postoperative complications, length of hospital stay, and 30-day mortality.
Interventions
PROCEDUREexperimental group
The music intervention consists of two parts. The first part occurs during the surgical procedure, starting from the induction of anesthesia and continuing until the surgery over. The second part spans from the first day post-surgery to the fifth day (or until discharge), with the patient listening to music twice a day, each session lasting for 30 minutes. The planned times for the music sessions are expected to be at 11 a.m. and 8 p.m. Each day post-surgery, the music intervention must be completed, and measurements of respiratory rate, pulse rate, blood pressure, and pain score should be taken both before and after listening to the music. Other are routine post-operative care.
Sponsors
Chang Gung Memorial Hospital
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Adults aged 65 years and above (inclusive). * Individuals with clear consciousness and willingness to participate in this study. * The primary treating physician of the participant must be the principal investigator or co-principal investigator of this study. * Diagnosis of femoral head fracture, femoral neck fracture, or intertrochanteric fracture. * Surgical procedures include hip hemiarthroplasty, total hip arthroplasty, cannulated screw fixation, dynamic hip screw, femoral neck system, and gamma-nail.
Exclusion criteria
* Bilateral hip fractures simultaneously. * History of neurosurgery. * Preoperative delirium. * Severe hearing impairment (unable to engage in oral conversation). * Use of sedatives or antidepressant medications. * Dementia or psychiatric disorders. * Patient unwilling to participate in the study or cooperate with listening to music (using headphones). * Use of unknown medications and alcohol. * After taking antihypertensive medication, preoperative systolic blood pressure \>200 mmHg or diastolic blood pressure \>110 mmHg. * Preoperative heart rate \>130 beats per minute or \<50 beats per minute.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| delirium event and severity | 7-14 days | Delirium is diagnosed based on clinical symptoms, utilizing the Confusion Assessment Method (CAM) to assess. CAM consists of four elements that can be quickly completed in a hospital setting, making it a convenient diagnostic tool. The four components include abrupt onset, fluctuating course of symptoms, inattention, and disorganized thinking or altered level of consciousness. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| opioid analgesic usage | 7-14 days | Comparison of patients' opioid analgesic dosage and frequency during hospitalization. |
| postoperative complications | 1 month | Comparison of surgical complications occurring during hospitalization or within one month post-discharge. |
| length of hospital stay | 7-14 days | Comparison of patients' length of hospital stay during hospitalization. |
| readmission within 14 days postoperatively | 1 month | Recording whether patients are readmitted within 14 days post-discharge due to surgical complications or delirium. |
| 30-day mortality | 1 month | Recording whether patients die within 30 days post-discharge due to surgical complications or delirium issues. |
Contacts
Primary ContactKu Han-Chang, Assistant Professor
Outcome results
None listed