Prospective, Assessment of Vitamin D and Calcium Supplementation, Improvement of Nutritional Status and Preoperative Rehabilitation in Patients Before Knee Arthroplasty.
2020년 2월 28일 업데이트: Bartlomiej Szpyra, Jagiellonian University
Prospective randomized study of 150 patients qualified for knee arthroplasty between 2015 and 2017. Patients were randomized into 3 groups receiving vitamin D and calcium supplementation, increased protein supply and preoperative rehabilitation, respectively.
Following factors were analyzed: changes in vitamin D3, calcium, total protein, albumin and CRP levels during preparation for surgery, nutritional status on the Subjective Global Assessment (SGA) scale, osteoporosis risk assessment according to the Osteoporosis Risk SCORE, level of pain felt on the scale VAS and the number of analgesics used, the result of the Duke Activity Status Index, the result of the following scales: Cardiac Risk Index for Orthopedic Surgery (Lee), Knee injury and Osteoarthritis Outcome Score (KOOS), Fear Avoidance Beliefs Questionnaire (FABQ) about Physical Activity, The Quality of Life Scale (QOLS). Additionally, the occurrence of perioperative complications was analyzed (e.g. venous thrombosis and pulmonary embolism, wound or joint infection, excessive bleeding, loosening of the implant, bone fracture or fracture, pain).
연구 개요
상태
상태
완전한
정황
정황
개입 / 치료
개입 / 치료
연구 유형
연구 유형
중재적
등록 (실제)
등록
150
단계
단계
- 해당 없음
연락처 및 위치
이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.
연구 장소
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Malopolska
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Kraków, Malopolska, 폴란드, 31-559
- Bartlomiej Szpyra
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참여기준
연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.
자격 기준
자격 기준
공부할 수 있는 나이
85년 이하 (어린이, 성인, 고령자)
건강한 자원 봉사자를 받아들입니다
아니
연구 대상 성별
모두
설명
Inclusion Criteria:
- with a disease lasting more than 5 years and without total limitation of physical fitness,
- reporting pain> 5 on the VAS scale (Visual Analogue Scale)
- general fitness according to the ASA (Amercican Society of Anestesiology) scale up to 3
Exclusion Criteria:
- patients with metabolic and systemic disorders with contraindications for calcium substitution, vitamin D3 and protein supply,
- intolerance of physical effort> 2, 5 MET (Metabolic Equivalent of Task)
- limitation of the degree overall efficiency> 3 in the ASA classification
공부 계획
이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 방지
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 하나의
팔의 수
3
무기와 개입
참가자 그룹 / 팔참가자 그룹 / 팔 |
개입 / 치료개입 / 치료 |
|---|---|
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활성 비교기: Intervention group 1
Protein supplementation BID, Vitamin D and calcium supplementation Vitamin D 2000 IU / d, calcium 1000mg/d, exercise 6 months
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Protein supplementation BID, Vitamin D and calcium supplementation Vitamin D 2000 IU / d, calcium 1000mg/d, exercise 6 months
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활성 비교기: Intervention group 2
Protein supplementation QD, Vitamin D and calcium supplementation Vitamin D 1000 IU / d, calcium 500mg/d, exercise 3 months
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Protein supplementation QD, Vitamin D and calcium supplementation Vitamin D 1000 IU / d, calcium 500mg/d, exercise 3 months
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위약 비교기: Control group 0
no protein supplementation , no Vitamin D and calcium supplementation , no exercise
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no protein supplementation , no Vitamin D and calcium supplementation , no exercise
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연구는 무엇을 측정합니까?
주요 결과 측정
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Pain control satisfaction assessed on the Visual Analogue Scale (VAS)
기간: 18 months
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Visual Analogue Scale (VAS) is a measure determining the intensity of pain by means of a visual analogue scale.
Subject is marking the examined point on a line of 10 cm long, where the value 0 is assigned the total absence of pain, and 10 the strongest pain that can be imagined.
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18 months
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Vitamin D concentration in blood, based on laboratory analysis.
기간: 18 months
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Concentration of vitamin D in blood is a laboratory parameter, measured in unit of ng/ml.
Levels below 20 ng/ml is a severe vitamin D deficiency condition that requires treatment.
The result in the range 20-30 ng/ml means that the vitamin level is not sufficient.
Values between 30-50 ng/ml are considered normal.
This is one of the basic laboratory parameters for assessing the body's bone mineral metabilism.
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18 months
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Efficiency of the knee joint assessed on The Knee Injury and Osteoarthritis Outcome Score (KOOS) scale.
기간: 18 months
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The Knee Injury and Osteoarthritis Outcome Score (KOOS) is a questionnaire designed to assess short and long-term patient-relevant outcomes following knee injury.
The KOOS is self-administered and assesses five outcomes: pain, symptoms, activities of daily living, sport and recreation function, and knee-related quality of life.
Scores are transformed to a 0-100 scale, with zero representing extreme knee problems and 100 representing no knee problems as common in orthopaedic scales and generic measures.
Scores between 0 and 100 represent the percentage of total possible score achieved.
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18 months
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2차 결과 측정
2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Calcium ionized concentration in blood, based on laboratory analysis.
기간: 18 months
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Calcium ionized concentration in blood is a laboratory parameter, measured in unit of mmol/l.
The results below 1.16 mmol/l mean that the level is not sufficient, condition called hypocalcemia.
Values between 1.16-1.32
mmol/l are considered normal.
The results above 1.32 mmol/l mean hypercalcemia occurs.
This is one of the basic laboratory parameters for assessing the body's bone mineral metabilism.
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18 months
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Total protein concentration in blood, based on laboratory analysis.
기간: 18 months
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Total protein concentration in blood is a laboratory parameter, measured in unit of g/l.
The results below 60 g/l mean that the level is not sufficient, condition called hypoproteinemia.
Values between 60-80 g/l are considered normal.
The results above 80 g/l mean hyperproteinemia occurs.
This is one of the basic laboratory parameters for assessing the body's nutritional status.
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18 months
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Albumin concentration in blood, based on laboratory analysis
기간: 18 months
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Albumin concentration in blood is a laboratory parameter, measured in unit of mg/ml.
The results below 35 mg/l mean that the level is not sufficient, condition called hypoalbuminemia.
Values between 35-50 mg/ml are considered normal.
The results above 50mg/l mean hyperalbuminemia occurs.
This is one of the basic laboratory parameters for assessing the body's nutritional status.
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18 months
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C-reactive protein (CRP) concentration in blood, based on laboratory analysis
기간: 18 months
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C-reactive protein concentration in blood is a laboratory parameter, measured in unit of mg/l.
The results below 5 mg/l are considered normal.
The results above 5mg/l mean infection, trauma, stress or other aggravating factor.
This is the major laboratory parameter for assessing homeostatic balance.
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18 months
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Efficacy of protein supplementation assessed on the Subjective Global Assessment (SGA) scale.
기간: 18 months
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Subjective global assessment (SGA) is the gold standard for diagnosing malnutrition.
SGA is a simple bedside questionnaire method used to diagnose malnutrition and identify those who would benefit from nutrition care.
The assessment includes taking a history of recent intake, weight change, gastrointestinal symptoms and a clinical evaluation.
Results are on a scale from 1 to 7. Values 1 and 2 means high risk of malnutririon, from 3 do 5 medium risk, and from 6 do 7 mild risk.
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18 months
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Efficacy of vitamin D and calcium supplementation assessed on the Simple Calculated Osteoporosis Risk Estimation (SCORE) scale.
기간: 18 months
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Simple Calculated Osteoporosis Risk Estimation (SCORE) scale is the questionnaire tool for diagnosing Osteoporosis risk.
It has been reported to appropriately identify person who should be referred for bone densitometry.
Results are on a scale from 0 to 50 points.
Points from 16 to 50 means high risk of osteoporosis , points from 7 to 15 moderate risk and from 0 do 6 low risk of osteoporosis.
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18 months
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Acceptability of physical activity based on Duke Activity Status Index (DASI) scale.
기간: 18 months
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The Duke Activity Status Index is a self-administered questionnaire that measures a patient's functional capacity.
It can be used to get a rough estimate of a patient's peak oxygen uptake.
Results are on a scale from 0 to 57,95 points.
The higher the score, the more intense the acceptable physical activity.
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18 months
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Incidence of cardiovascular hazard based on Cardiac Risk Index for Orthopedic Surgery (Lee) scale.
기간: 18 months
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Cardiac Risk Index for Orthopedic Surgery (Lee) is the questionnaire tool for diagnosing cardiovascular hazard in orthopedics patients.
Results are on a scale from 0 to 6 points.
Points from 3 to 6 means estimated risk of 4%, 2 points is 2,3% of risk, 1 point is 1,7% of risk and 0 points means less than 1 % of cardiovascular event.
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18 months
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Unwillingness of phisical activity due to pain based on Fear Avoidance Beliefs Questionnaire (FABQ) scale.
기간: 18 months
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Fear Avoidance Beliefs Questionnaire (FABQ) scale is a questionnaire based on the Fear-Avoidance Model of Exaggerated Pain Perception, a model created in attempts to explain why some patients with acute painful conditions can recover while other patients develop chronic pain from such conditions.
The FABQ focuses specifically on how a patient's fear-avoidance beliefs about physical activity and work.
It consists of 16 questions scaled form 0 do 6, higher score indicates fear avoidance behaviors.
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18 months
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The Quality of Life based on The Quality of Life (QOLS) scale.
기간: 18 months
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The Quality of Life (QOLS) scale is the most known scale measures factors like satisfaction, perceptions of control, involvement, commitment, and work-life balance, in terms of one's personal perception.
QOLS has 16 items, scaled form 1 do 7, higher score indicates superior appraisal of each aspect of life.
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18 months
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Incidence of Treatment-Emergent Adverse Events (AE) as assessed by frequency.
기간: 18 months
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Incidence of Adverse Events (AE) was summed up and analyzed in each group. They were divided into 7 groups.
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18 months
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공동 작업자 및 조사자
여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.
연구 기록 날짜
이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.
연구 주요 날짜
연구 시작 (실제)
연구 시작
2015년 1월 1일
기본 완료 (실제)
기본 완료
2017년 12월 31일
연구 완료 (실제)
연구 완료
2017년 12월 31일
연구 등록 날짜
최초 제출
최초 제출
2020년 2월 27일
QC 기준을 충족하는 최초 제출
QC 기준을 충족하는 최초 제출
2020년 2월 28일
처음 게시됨 (실제)
처음 게시됨
2020년 3월 2일
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
마지막 업데이트 게시됨
2020년 3월 2일
QC 기준을 충족하는 마지막 업데이트 제출
QC 기준을 충족하는 마지막 업데이트 제출
2020년 2월 28일
마지막으로 확인됨
마지막으로 확인됨
2020년 2월 1일
추가 정보
이 연구와 관련된 용어
추가 관련 MeSH 약관
기타 연구 ID 번호
기타 연구 ID 번호
- KBET/271/B/2014
개별 참가자 데이터(IPD) 계획
개별 참가자 데이터(IPD)를 공유할 계획입니까?
아니요
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
아니
미국 FDA 규제 기기 제품 연구
아니
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