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Silkeborg Knee Replacement Cohort Study

2022年3月30日 更新者:Central Jutland Regional Hospital
In this cohort study, we will investigate short and long term outcomes after knee replacement surgery and identify preoperative and early postoperative factors associated with long term outcome.

研究概览

详细说明

All patients follow the same fast-track program including same day surgery for elective knee replacement surgery at the Silkeborg Regional Hospital in Denmark, which includes detailed preoperative written information, multidisciplinary education course for patients and relatives, optimized multimodal pain treatment and early postoperative rehabilitation. Before the admission for surgery, patients will be asked to fulfill several questionnaires and baseline information regarding work situation, educational level and previous treatments. At two weeks there, there is a scheduled follow up by a physical therapist and a nurse at the hospital. At three months there is a scheduled follow up by telephone with a physical therapist.

The study will adhere methodologically to the STROBE guidelines and checklist for prospective cohort studies (www.strobe-statement.org).

Further description is provided elsewhere as eligibility criteria and outcome measures.

Addition to the description:

In January 2019 we started collecting 1 year follow-up data and included questions regarding treatment success, satisfaction and willingness to repeat the surgery.

In March 2019 we decided to make a change in the baseline collection of relevant predictors for primary outcome. The reason for the change was to be able to answer more relevant scientific questions in the cohort study. We replaced "The General Self-efficacy Scale" with "Pain Catastrophizing Scale" and excluded "The General Self-efficacy Scale" from the 12 weeks follow-up collection of outcome measures.

March 2020:

The SIKS study was planned to continue recruitment until reaching minimum 1,000 TKA patients with follow-up data which was deemed sufficient for the purpose of the planned studies. In March 2020, the COVID-19 pandemic closed down all elective orthopaedic surgeries. Because of that, we decided to stop the recruitment to the cohort study with the last patient included (at March 16th, 2020, prior to the COVID-19 lockdown).

December 2020:

The first substudies are planned using data from the SIKS cohort:

  1. Predictors of knee pain and functional outcome following Total Knee Arthroplasty - a prospective cohort study with 12 months follow up

    Primary outcome:

    Oxford Knee Score at 12 months

  2. Is it feasible and safe to discharge patients on the day of surgery after a total knee arthroplasty?

    Primary outcomes Feasibility measured as length of stay Safety measures as readmission (phone calls, outpatient visits and inpatient visits) and the related reason

    Secondary outcomes Oxfort knee score (90 days) Pain intensity (90 days)

  3. Associations between preoperative BMI and postoperative physical activity level and functional capacity 12 months after UKA or TKA surgery.

Primary outcome UCLA scale (12 months)

Secondary outcomes Oxford Knee Score (12 months)

研究类型

观察性的

注册 (实际的)

1225

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • Jutland
      • Silkeborg、Jutland、丹麦、8600
        • Silkeborg Regional Hospital

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 及以上 (成人、年长者)

接受健康志愿者

有资格学习的性别

全部

取样方法

概率样本

研究人群

Patients assigned for primary knee replacement in the period from February 2018 to May 2020 will be consecutively recruited to the cohort from Silkeborg Regional Hospital Denmark.

描述

Inclusion Criteria:

  • Assigned for primary Unicompartmental or Total Knee Replacement
  • Age ≥ 18 years at the time of recruitment
  • Able to read and understand Danish

Exclusion Criteria:

  • Not mentally able to reply to the questionnaire

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

队列和干预

团体/队列
干预/治疗
Knee replacement
Patients assigned for total or unicompartmental knee replacement surgery
Fast-track Knee replacement surgery including same day surgery

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Oxford Knee Score (OKS) (continous)
大体时间:52 weeks after surgery
Disease specific Patient Reported Outcome Measure regarding function and pain. Each question is answered by ticking a box on a five-point Likert scale. Responses are then totalled to obtain a score between 0 and 48, with 48 being the best.
52 weeks after surgery

次要结果测量

结果测量
措施说明
大体时间
Oxford Knee Score (OKS) (continous)
大体时间:Pre surgery
Disease specific Patient Reported Outcome Measure regarding function and pain. Each question is answered by ticking a box on a five-point Likert scale. Responses are then totalled to obtain a score between 0 and 48, with 48 being the best.
Pre surgery
Oxford Knee Score (OKS) (continous)
大体时间:12 weeks after surgery
Disease specific Patient Reported Outcome Measure regarding function and pain. Each question is answered by ticking a box on a five-point Likert scale. Responses are then totalled to obtain a score between 0 and 48, with 48 being the best
12 weeks after surgery
EQ-5D-5L (continous)
大体时间:Pre surgery
Generic Health Related Quality of Life Patient Reported Outcome Measure
Pre surgery
EQ-5D-5L (continous)
大体时间:12 weeks after surgery
Generic Health Related Quality of Life Patient Reported Outcome Measure
12 weeks after surgery
EQ-5D-5L (continous)
大体时间:52 weeks after surgery
Generic Health Related Quality of Life Patient Reported Outcome Measure
52 weeks after surgery
The General Self-efficacy Scale (continous)
大体时间:Pre surgery
A generic Patient Reported Outcome Measure. The General Self-efficacy Scale measures self-efficacy, defined as an individual's belief in his or her capacity to execute behaviors necessary to produce specific performance attainments.Each question is answered by ticking a box on a four-point Likert scale. Responses are then totalled to obtain a score between 10 and 40, with 40 being the best. he General Self-efficacy Scale measures self-efficacy, defined as an individual's belief in his or her capacity to execute behaviors necessary to produce specific performance attainments.Each question is answered by ticking a box on a four-point Likert scale. Responses are then totalled to obtain a score between 10 and 40, with 40 being the best. The General Self-efficacy Scale is included in the data collection from January 2019 til March 2019, which corresponds to about 550 patient responds.
Pre surgery
The General Self-efficacy Scale (continous)
大体时间:12 weeks after surgery
A generic Patient Reported Outcome Measure. The General Self-efficacy Scale measures self-efficacy, defined as an individual's belief in his or her capacity to execute behaviors necessary to produce specific performance attainments. Each question is answered by ticking a box on a four-point Likert scale. Responses are then totalled to obtain a score between 10 and 40, with 40 being the best. The General Self-efficacy Scale is included in the data collection from January 2019 til June 2019, which corresponds to about 550 patient responds
12 weeks after surgery
Pain Visual Analog Scale (VAS) (continous)
大体时间:Pre surgery
Measured in rest and activity. The pain VAS is a generic pain measure on a continuous scale comprised of a horizontal line orientated from the left (worst) to the right (best), 100 mm in length
Pre surgery
Pain Visual Analog Scale (VAS) (continous)
大体时间:12 weeks after surgery
Measured in rest and activity. The pain VAS is a generic pain measure on a continuous scale comprised of a horizontal line orientated from the left (worst) to the right (best), 100 mm in length
12 weeks after surgery
Pain Visual Analog Scale (VAS) (continous)
大体时间:52 weeks after surgery
Measured in rest and activity. The pain VAS is a generic pain measure on a continuous scale comprised of a horizontal line orientated from the left (worst) to the right (best), 100 mm in length
52 weeks after surgery
Analgetic pain medication intake (type and frequence)
大体时间:Pre surgery
Self-reported by the patients
Pre surgery
Analgetic pain medication intake (type and frequence)
大体时间:12 weeks after surgery
Self-reported by the patients
12 weeks after surgery
Analgetic pain medication intake (type and frequence)
大体时间:52 weeks after surgery
Self-reported by the patients
52 weeks after surgery
Range of Motion (ROM) in passive knee flexion and passive knee extension (degrees)
大体时间:Pre surgery
Measures is conducted by a doctor
Pre surgery
UCLA Activity Scale (continuous)
大体时间:Pre surgery
Patient Reported Outcome Measure, that measures physical activity in patients with knee replacements on a 10-level scale, where "10" is very active
Pre surgery
UCLA Activity Scale (continuous)
大体时间:12 weeks after surgery
Patient Reported Outcome Measure, that measures physical activity in patients with knee replacements on a 10-level scale, where "10" is very active
12 weeks after surgery
UCLA Activity Scale (continuous)
大体时间:52 weeks after surgery
Patient Reported Outcome Measure, that measures physical activity in patients with knee replacements on a 10-level scale, where "10" is very active
52 weeks after surgery
Pain Catastrophizing Scale (PCS)
大体时间:Pre surgery
Patient Reported Outcome Measure, that measures how patients experience pain. Pain catastrophizing is characterized by the tendency to magnify the threat value of a pain stimulus and to feel helpless in the presence of pain, as well as by a relative inability to prevent or inhibit pain-related thoughts in anticipation of, during, or following a painful event such as surgery for example. Each of the 13 questions is answered by ticking a box on a 5 point Likert Scale from 0 (not at all) to 4 (all the time). A total score is yielded (ranging from 0-52 and 0 being the best), along with three subscale scores assessing rumination, magnification and helplessness. The PCS is included in the data collection from March 2019 til end of the cohort study, which corresponds to about 950 patient responses (instead of The General Self-efficacy Scale)
Pre surgery
Global Perceived Effect (GPE)
大体时间:52 weeks after surgery
GPE measures patients' perception of the change in their knee problems after the surgery. GPE will be assessed with the anchor question "Overall, how are the problems now (pain and ability to perform daily activities) in the knee on which you had surgery, compared to prior to your operation?" Patients respond on a 7-point scale ranging from "better, an important improvement" to "worse, an important deterioration".
52 weeks after surgery
Satisfaction with the surgery
大体时间:52 weeks after surgery
Satisfaction is measured with the question "Overall, how satisfied are you with the sugery?". Patients respond on a 5 point scale ranging from "very satisfied" to "very unsatisfied"
52 weeks after surgery
Patient Acceptable Symptom State (PASS)
大体时间:52 weeks after surgery
PASS measures satisfaction with the current knee function and will be assessed with the anchor question ""When you think of your knee function, will you consider your current condition as satisfying? With knee function, you should take into account your activities of daily living, your level of pain and other symptoms". Patients respond "yes" or "no". If patients respond "no" they are asked if the consider the treatment of ther knee problem as a failure.
52 weeks after surgery
Global assessment of willingness to repeat the surgery
大体时间:52 weeks after surgery
Assessed with the anchor question "knowing what your knee arthroplasty surgery did for you, if you could go back in time, would you still have undergone this surgery?" Patients respond "yes", "no" or "uncertain".
52 weeks after surgery
Feasibility (length of stay)
大体时间:2 weeks after surgery
Measured as length of stay and reason for not being discharged on post operative day 0 (same-day) will be provided.
2 weeks after surgery
Safety (readmission)
大体时间:1) 2 weeks after surgery, 2) 2 weeks after surgery, and 3) 90 days after discharge
  1. number of patient-initiated phone calls
  2. number of unscheduled visits in the outpatient clinic
  3. number of inpatient readmission (admission to hospital ward taking up a bed)
1) 2 weeks after surgery, 2) 2 weeks after surgery, and 3) 90 days after discharge
Safety (complications)
大体时间:1) 2 weeks after surgery, 2) 2 weeks after surgery, and 3) 90 days after discharge

The reason for readmission (=complication) in relation to:

  1. patient-initiated phone calls
  2. unscheduled visits in the outpatient clinic
  3. inpatient readmission (admission to hospital ward taking up a bed) will be reported.
1) 2 weeks after surgery, 2) 2 weeks after surgery, and 3) 90 days after discharge

其他结果措施

结果测量
措施说明
大体时间
Pain Visual Analog Scale (VAS) (continous)
大体时间:2 weeks after surgery
Measured in rest and activity. The pain VAS is a generic pain measure on a continuous scale comprised of a horizontal line orientated from the left (worst) to the right (best), 100 mm in length
2 weeks after surgery
Analgetic pain medication intake (type and frequence)
大体时间:2 weeks after surgery
Registrated by a nurse
2 weeks after surgery
Range of Motion (ROM) in passive knee flexion and passive knee extension (degrees)
大体时间:2 weeks after surgery
Measures is conducted by a physical therapist
2 weeks after surgery
Range of Motion (ROM) in passive knee flexion and passive knee extension (degrees)
大体时间:pre surgery
Measures is conducted by a doctor
pre surgery

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Lone Ramer Mikkelsen, Msc., Ph.D.、Interdisciplinary Research Unit Elective Surgery Centre Silkeborg Regional Hospital, Denmark
  • 首席研究员:Mette Garval, PT, Msc.、Physical Therapy Department, Elective Surgery Centre Silkeborg Regional Hospital, Denmark
  • 学习椅:Søren Thorgaard Skou, PT, PhD、Research Unit for Musculoskeletal Function and Physiotherapy University of Southern Denmark
  • 首席研究员:Anne Mette Schmidt, Msc., Ph.D.、Interdisciplinary Research Unit Elective Surgery Centre Silkeborg Regional Hospital, Denmark

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2018年2月1日

初级完成 (实际的)

2021年3月23日

研究完成 (实际的)

2021年3月23日

研究注册日期

首次提交

2018年1月19日

首先提交符合 QC 标准的

2018年1月19日

首次发布 (实际的)

2018年1月25日

研究记录更新

最后更新发布 (实际的)

2022年4月8日

上次提交的符合 QC 标准的更新

2022年3月30日

最后验证

2020年5月1日

更多信息

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