Effectiveness of a Prehabilitation Program on Clinical, Functional and Psychological Variables in Candidates for Hip or Knee Arthroplasty Surgery.
概览
- 阶段
- 不适用
- 干预措施
- Prehabilitation Program
- 疾病 / 适应症
- Prehabilitation
- 发起方
- University of Jaén
- 入组人数
- 44
- 试验地点
- 1
- 主要终点
- Measuring Quality of life
- 状态
- 招募中
- 最后更新
- 2个月前
概览
简要总结
We live in an increasingly aging society in which the incidence of osteoarticular diseases increases, among which osteoarthritis (OA) stands out. OA is a degenerative disorder of the different components of the joint leading to a progressive destruction of the same. The hip and knee being the most affected joints, OA presents multiple symptoms such as pain, stiffness and functional limitation, also causing psychological disorders such as anxiety, depression, quality of sleep and poor perception of quality of life. Conventional treatment is aimed at alleviating symptoms, but when conservative therapies fail in the more advanced stages of the disease, total joint replacement surgery or arthroplasty is the therapeutic option of choice. Strength physical exercise (PE) and aerobic training have been shown to be effective in OA, obtaining positive effects on the symptoms and on variables that deteriorate this disease. The concept of pre-habilitation or preoperative rehabilitation has been shown through other studies in different pathologies (cardiopulmonary and musculoskeletal) to have positive effects at a clinical and functional level, however, the planning of a pre-habilitation protocol in hip or knee arthroplasty is still controversial.
The purpose of this study is to determine the effect that a prehabilitation program will produce and its possible usefulness in those subjects who are waiting for a hip or knee arthroplasty. It is expected to find favorable results that support this therapy when it comes to reducing postoperative recovery times, functional capacity and other psychological variables of interest.
This powerful tool could represent a non-pharmacological and non-invasive therapy, as well as being useful and economical in the management of patients with OA in advanced stages.
研究者
Irene María Lopera Pareja
Principal Investigator
University of Jaén
入排标准
入选标准
- •Diagnosis of hip OA stage I-III of the Tönnis classification or diagnosis of knee OA stage I-IV of the Ahlbäck classification
- •Patients requiring hip/knee arthroplasty surgery
- •Signed informed consent
- •Obtaining a score equal to or greater than 8 repetitions in the Sit to Stand test
- •Patients with the ability to walk without technical aids or in need of some help (up to two canes or a walker)
排除标准
- •Cognitive deficit/Dementia states
- •Cancer processes
- •Associated vascular and inflammatory pathologies
- •Associated neurological pathologies
- •Contraindications to physical exercise
研究组 & 干预措施
Intervention Group
The intervention group (IG) will undergo a 6-week prehabilitation program for total hip/knee replacement surgery. Once the surgery is complete, they will follow the same rehabilitation program proposed for the control group.
干预措施: Prehabilitation Program
Control Group
The control group (CG) will carry out a post-operative physiotherapy program in addition to a home exercise program that will be shown by the physiotherapist before hospital discharge.
干预措施: Non prehabilitation Program
结局指标
主要结局
Measuring Quality of life
时间窗: Start of the study and week 24
SF-12 Health Questionnaire: This is a valid instrument for measuring health-related quality of life (HRQoL). The SF-12 is a reduced version of the SF-36 questionnaire, consisting of a subset of 12 items from the SF-36, selected by multiple regression, including 1 or 2 items from each of the 8 domains of the SF-36. From the information obtained from these 12 items, the SF-12 physical and mental summary measures are obtained as the only assessments. The assessments vary between 0 (no quality of life) and 100 (maximum quality of life).
次要结局
- Lower limb functionality(Start of study, week 6, week 9 and week 24.)
- Level of perceived exertion(From the start of the prehabilitation program until 6 weeks (end of the prehabilitation program))
- Intensity of Pain(Start of the intervention, week 6, week 9 and week 24.)
- Psychological aspects(Start of intervention, week 6 and week 24.)
- Sleep Quality(Start of the intervention and week 24)
- Analgesic consumption(Start and week 6.)
- Therapeutic adherence(Start of the intervention and week 6.)
- Treatment expectations and therapeutic satisfaction(24/48 hours post-surgery)
- Independent values(All were measured at the start of the intervention and at week 24.)
- Independent Values: Weight(The start of the intervention, week 6, week 9 and at week 24.)
- Independent Values: Height(The start of the intervention and at week 24.)
- Independent Values: body mass index (BMI)(The start of the intervention, week 6, week 9 and at week 24.)
- Independent Values: general analytical and biochemical parameters(The start of the intervention and at 24/48 hours after surgery)
- Strength(Start of the study, week 6, week 9 and week 24 (end of the intervention))
- Lower limb functionality(Start of study, week 6, week 9 and week 24)
- Strength(Start of study, week 6, week 9 and week 24 (end of intervention).)