Clinical Trials Logo

Clinical Trial Summary

Objective: This study will be conducted to determine the effect of early mobilization on pain and mobility levels in patients who underwent total knee prothesis. Method: This study, which was designed as a randomized controlled experimental type, will be conducted with a total of 68 patients, 34 of whom were in the control group and 34 in the experimental group, who underwent total knee prothesis surgery in the orthopedics and traumatology service at Bartın State Hospital between September 2022 and June 2023. Research data will be collected with Participant Information Form, Brief Pain Inventory, Patient Mobility Scale and Observer Mobility Scale. During the data collection process, the pain level of the experimental group will be evaluated at the 8th hour after the operation, then the level of mobility will be evaluated by providing mobilization. The control group will only be evaluated for pain at the 8th hour after surgery, and they will not be mobilized. At the 20th hour after the surgery, pain assessment of both groups will be made, and then their mobility will be evaluated, and their mobility levels will be evaluated. SPSS 22.0 program will be used in the evaluation of the data. Whether the data is normally distributed or not will be tested by Shapiro-wilk analysis. According to the result of this, parametric and nonparametric methods will be used.


Clinical Trial Description

Introduction: Pain development is an expected situation in individuals who have undergone total knee replacement surgery. Again, in these patients, the tendency to stay still increases due to the surgery and pain. International guidelines and other studies indicate that early mobilization of patients after surgical interventions is effective in preventing complications that can be caused by inactivity and reducing the severity of pain in patients. Early mobilization gains importance in order to accelerate the recovery process of patients after total knee replacement surgery and to prevent problems such as muscle mass loss and muscle weakness that may arise from long-term bed rest. Objective: This study will be conducted to determine the effect of early mobilization on pain and mobility levels in patients who underwent total knee replacement. Method: This study, which was designed as a randomized controlled experimental type, will be conducted with a total of 68 patients, 34 of whom were in the control group and 34 in the experimental group, who underwent total knee replacement surgery in the orthopedics and traumatology service at Bartın State Hospital between September 2022 and June 2023. Research data will be collected with Participant Information Form, Brief Pain Inventory, Patient Mobility Scale and Observer Mobility Scale. The patients in the experimental group will not be mobilized until the 8th hour, and their first mobilization will be carried out at the 8th hour. The pain levels of the patients in the experimental group at the 8th hour will be evaluated with the Brief Pain Inventory and their mobilization will be ensured. Mobility levels after mobilization will be recorded by evaluating with the Patient Mobility Scale and by the research nurse who mobilized the patient with the Observer Mobility Scale. Patients in the control group will not be mobilized until the 20th hour after surgery. Patients will be evaluated only for pain at the 8th hour after surgery. The first mobilizations will be made at the 20th hour after the surgery, and their mobility levels will be evaluated with the Observer Mobility Scale and the Patient Mobility Scale by both the patient and the researching nurse who mobilized them. Pain assessment will be performed in both groups at the 20th hour and then their mobility will be evaluated. SPSS 22.0 program will be used in the evaluation of the data. Whether the data is normally distributed or not will be tested by Shapiro-wilk analysis. According to the result of this, parametric and nonparametric methods will be used. Conclusion: If the research is carried out successfully, the differences caused by early mobilization in the pain levels and mobility levels of the patients will be revealed. The fact that early mobilization causes a decrease in the level of pain, as stated in the literature, will enable patients to be mobilized earlier. Again, if early mobilization has a positive effect on the mobility level of the patients, the patients will be able to be mobilized early for this purpose. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05587985
Study type Observational [Patient Registry]
Source Bartin University
Contact Mediha Didem KOCOGLU
Phone 5070300248
Email mdidemkocoglu@gmail.com
Status Not yet recruiting
Phase
Start date November 1, 2022
Completion date October 1, 2023

See also
  Status Clinical Trial Phase
Completed NCT06053957 - The Effect of Early Mobilization on Postoperative Recovery in Abdominal Surgery N/A
Completed NCT03300336 - Optimizing Function and Independence Through STRIDE N/A
Completed NCT04423796 - Robotic Assisted Early Mobilization in Ventilated ICU Patients N/A
Active, not recruiting NCT03888027 - WalkMORE: A Volunteer-driven Walking Intervention N/A
Recruiting NCT06212622 - Is the Rate of Early Mobilisation in Hip Fracture Patients Using Alfentanil Better Than Standard Opioid Analgesia?
Completed NCT03361891 - WalkMORE: Volunteer Walking Coach Program for Hospitalized Internal Medicine Patients N/A
Recruiting NCT06436508 - The Investigation of the Impact of Early Mobilization on the Outcome in Patients With Aneurysmal Subarachnoid Hemorrhage. N/A
Active, not recruiting NCT04868656 - Implementing a Hospital-Based Walking Program (STRIDE): Function QUERI 2.0 N/A
Recruiting NCT03175783 - Use of Wearable Activity Tracker in Elderly Undergoing Abdominal Surgery N/A
Completed NCT03314623 - Immediate Mobilization After Plate Osteosynthesis of Proximal Tibial Fractures - A Cohort Study
Completed NCT02980926 - Mepivacaine vs. Bupivacaine Spinal Anesthetic in Total Knee Arthroplasty Phase 4
Completed NCT01045330 - a Modified NTU-HELP Program N/A