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临床试验/NCT05389800
NCT05389800尚未招募不适用

Pre- and Post-Operative Effects of Upper Extremity Aerobic Exercise in Mobility, Haemostatic Balance, and Mortality- and Morbidity-related Biomarkers in Hip Fracture Patients: A Randomized Controlled Trial

National and Kapodistrian University of Athens2 个研究点 分布在 1 个国家目标入组 116 人开始时间: 2024年7月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
116
试验地点
2
主要终点
Six Minute Walk Test (6MWT)

研究概览

简要总结

The purposes of this study are to determine the benefits of a pre-operative aerobic exercise program and an 8-week postoperative aerobic exercise program with a portable upper extremity cycle-ergometer in patients with hip fracture.

详细描述

Hip fracture is one of the primary causes of significant morbidity in those over than 65 years old. Hip fracture is also among the top ten causes of loss of disability-adjusted life years in elderly. For the year 2020, in terms of the percentage of population over 80 years, Greece was second among the countries of the European Union, with this age group constituting 7.2% of its total population. In Greece, between 1977 and 2007, hip fractures doubled, with the annual impact rising to 343.96 per 100,000 inhabitants. For this population, a critical part of management is physical activity and exercise prescription both to prevent complications and to enhance rehabilitation after surgery. Postoperative (post-discharge) aerobic exercise programs of moderate intensity have already been used in patients with hip fracture proving its safety and positive effect in a variety of outcomes, such as aerobic capacity and quality of life. It is well established that these patients do not meet the minimum least amount of activity that should be done per week, based on Guidelines for Physical Activity by the World Health Organization neither during their hospitalization nor during their later life in the community. Also, although most Clinical Guidelines recommend a surgical management within 48 hours after hip trauma, there are many patient and system factors which can contribute to delayed surgery, such as surgical readiness, available resources, prioritisation and out-of-hours admission.

In terms of pre-operative exercise program, the investigators hypothesize that it will reduce surgical stress through the body's better response to lactate accumulation and the acute physiological effects on the patient's hematopoietic activity and hemostatic profile. Moderate intensity exercise will reduce platelet hyperactivity, increase fibrinolytic activity and reduce coagulation factors. In this more favorable environment, the immediate postoperative recovery of basic mobility can be accelerated. Regarding the post-operative exercise program, the investigators hypothesize that it will improve the independence and function of the lower extremity by increasing the cardiopulmonary capacity, while the improvement of the nutritional factors (albumin and pre-albumin) through the post-training protein synthesis will also contribute to this.

Apart from primary and secondary outcomes, at baseline the investigators will also evaluate the following: demographics; characteristics about the fracture and upcoming surgery, such as the type of fracture and the surgical procedure; New Mobility Score (NMS) to define the prefracture functional level; Addenbrooke's Cognitive Examination - III (ACE-III) to define the cognitive status.

The power analysis for the selection of the sample size for the postoperative program in the change of the 6-Minute Walk Test (primary outcome) after the completion of the program, in the 8 weeks postoperatively, was performed for significance level α = 0.05 and power = 90%.The investigators' assumption for power analysis stands to find a difference of 50 meters between the groups. Considering that the ratio between the groups will be 1: 1, the required sample size is 96 patients (48 in each group). Adding a drop-out rate of 20%, required sample size is defined in 116 patients (58 in each group). About the other primary outcome (postoperative 3-day Cumulated Ambulation Score - CAS), the investigators' power analysis revealed a required sample size of 80 patients, based on the assumptions of 2.4 points difference between the groups, α = 0.05 and power = 90%. In statistical analysis, only patients who completed at least a 3 days of preoperative program will be included.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
65 Years 至 —(Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age: 65 years old and older
  • Unilateral proximal femoral fracture/hip fracture (intertrochanteric or neck fracture)
  • Ambulatory patients before fracture (with or without aid assistance)
  • Agreed to participate and signed consent form

排除标准

  • Pathological fractures (under musculoskeletal oncology)
  • Severe neuropsychiatric disorder (eg severe psychiatric disorder, dementia, etc.) to the extent that the researcher deems the patient incompetent or likely unable to remain compliant with the follow-up
  • Unable to implement the exercise program due to underlying pathology or disability in the upper extremities
  • More than one fracture
  • Severe and / or unstable cardiovascular disease [e.g. congenital heart disease, uncontrolled severe hypertension (systolic blood pressure ≥ 180 mmHg and / or diastolic blood pressure ≥ 120 mmHg), unstable angina]
  • Neurological or other conditions that significantly impair function and independence (eg stage 3-5 Parkinson's disease according to Hoehn and Yahr, advanced Multiple Sclerosis, severe arthritis of degenerative or rheumatic etiology)
  • Severe metabolic bone disease (eg Paget's disease, renal bone disease, osteomalacia), excluding osteoporosis
  • Active deadly aggressive disease (eg end-stage cancer with an estimated survival expectancy of less than 6 months)
  • Unable to understand the consent document and / or protocol instructions
  • Refusal to participate in the research

研究组 & 干预措施

Aerobic Exercise (Moderate-Intensity Interval Training)

Experimental

Preoperative program: 120 seconds of moderate intensity exercise (64-76% HRmax, 12-13 in rate of perceived exertion (RPE), based on ACSM) and 120 seconds of passive rest in a total of 4 cycles. The basic program will last about 14 minutes, plus 6 minutes for warm-up and recovery. The program will be performed twice a day.

Postoperative program: 120 seconds of moderate intensity exercise (64-76% HRmax, 12-13 in RPE, based on ACSM) and 120 seconds of passive rest in a total of 8 cycles. The basic program will last about 30 minutes, plus 6 minutes for warm-up and recovery. The program will be performed 3 times a week for a total of 8 weeks.

干预措施: Upper Extremity Aerobic Exercise (Other)

Control

No Intervention

Preoperatively: mild intensity activities focusing on memory and attention performing with upper limb movements using the interactive platform Kinems. The program will last about 20 minutes. To ensure that the intensity of activities is mild, there will be a simultaneous recording of heart rate, while at the end of each session the RPE scale will be evaluated.

Postoperatively: none

结局指标

主要结局

Six Minute Walk Test (6MWT)

时间窗: 8 weeks post-operatively

The 6MWT is a sub-maximal exercise test that is used to determine aerobic capacity and endurance.

Cumulated Ambulation Score

时间窗: Total 3-day Cumulated Ambulation Score post-operatively.

The Cumulated Ambulation Score (CAS) is a reliable and valid instrument for assessing patients' basic mobility (getting in and out of bed, sit-to-stand from a chair, and walking), in orthopaedic wards. The minimum value is 0 and maximum 3 per day. The total 3-day CAS has a better prognostic value than the 1-day CAS, and is based on the sum score of the first three post-operative days, with a minimum value being 0 and maximum 9, for the total 3-day CAS, with a higher score means better outcome.

次要结局

  • Lower Extremity Functional Scale(At admission (for pre-operative status) and 4, 8, 26 & 52 weeks post-operatively (for current status))
  • Lactate levels(Day 0 (at admission), Intraoperatively (at the beginning, 30 minutes later, and at the end of the surgery), & 12h postoperatively)
  • Albumin levels(First day of admission, one day before surgery, 3 days, 4, 8, 26 & 52 weeks post-operatively)
  • Cumulated Ambulation Score(4 weeks post-operatively)
  • Six Minute Walk Test (6MWT)(4, 26 & 52 weeks post-operatively)
  • Timed-Up & Go(4, 8, 26 & 52 weeks post-operatively)
  • Modified Harris Hip Score(At admission (for pre-operative status) and 4, 8, 26 & 52 weeks post-operatively (for current status))
  • Tissue plasminogen activator(First day of admission, one day before surgery, 3 days, 1, 4, 8, 26 & 52 weeks post-operatively)
  • Plasminogen activator inhibitor-1(First day of admission, one day before surgery, 3 days, 1, 4, 8, 26 & 52 weeks post-operatively)
  • Thrombin-Antithrombin Complex(First day of admission, one day before surgery, 3 days, 1, 4, 8, 26 & 52 weeks post-operatively)
  • Endogenous Thrombin Potential(First day of admission, one day before surgery, 3 days, 1, 4, 8, 26 & 52 weeks post-operatively)
  • Fibrinogen plasma levels(First day of admission, one day before surgery, 3 days, 1, 4, 8, 26 & 52 weeks post-operatively)
  • D-Dimers plasma levels(First day of admission, one day before surgery, 3 days, 1, 4, 8, 26 & 52 weeks post-operatively)
  • Thrombomodulin plasma levels(First day of admission, one day before surgery, 3 days, 1, 4, 8, 26 & 52 weeks post-operatively)
  • Transfusion requirements (litre)(Post-operative day 1, 2 and 3)
  • Re-admission(4, 8, 26 & 52 weeks post-operatively)
  • Haemostatic profile using ROTEM(First day of admission, one day before surgery, 3 days, 1, 4, 8, 26 & 52 weeks post-operatively)
  • von Willebrand factor (VWF); VWF:Antigen and VWF:Activity plasma levels(First day of admission, one day before surgery, 3 days, 1, 4, 8, 26 & 52 weeks post-operatively)
  • Deep vein thrombosis & Pulmonary embolism (DVT & PE)(4, 8, 26 & 52 weeks post-operatively)
  • All-cause mortality(4, 8, 26 & 52 weeks post-operatively)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Panagiotis Koulouvaris

MD, Assistant Professor, 1st Department of Orthopaedic Surgery, National and Kapodistrian University of Athens

National and Kapodistrian University of Athens

研究点 (2)

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