機能的困難に関するアンケートの短縮版: トルコ語翻訳、妥当性および信頼性の研究。
機能的困難に関するアンケートの短縮版調査のトルコ語への適応と心理測定特性の決定: 妥当性と信頼性の研究。
The Functional Difficulties Questionnaire-shortened version "(FDQ-s) is a unique questionnaire that aimed at evaluating the functional performance of the upper extremities and trunk following cardiothoracic surgery.
Aim of this study is adaptation of the FDQ-s questionnaire to Turkish culture and study its psychometric properties, validity and reliability.
調査の概要
状態
状態
条件
条件
詳細な説明
Cardiac surgeries performed by sternotomy method are the most common surgical treatment method in coronary artery disease. Although the median sternotomy has advantages in terms of ease of application, cost and long-term survival, muskuloskeletal complications can be encountered in the postoperative period.
In the studies conducted, it was found that patients had difficulties in functional activities including mobilization and daily life activities after median sternotomy. Also restrictions or loss of motion can be observed in the joint range of motion of the shoulder joint and thoracic region.
The FDQ-s scale consists of 10 functional tasks developed by Sturgess et al. These tasks are activities such as coughing, sneezing, deep breathing, movements involving the upper extremity, turning in bed, sitting upright in the chair, and ambulation. When applying FDQ-s, patients will mark how hard they are in each task on the 100 mm straight line. The first point on the left means "no difficulty" and the last point on the right means "maximum difficulty". The score will be determined by measuring from the starting point to the place marked by the patient. The total score is at most 100 points and at least 0 points. The high score indicates that the patient's difficulty level is high.
Although there are many functional difficulties faced by patients in the postoperative period, there is no outcome measurement in our language that evaluates the level of these difficulties globally and objectively.
Our research will be done due to the elimination of this deficiency in the literature.
研究の種類
研究の種類
入学 (実際)
入学
連絡先と場所
研究場所
-
-
-
Aydin、トルコ（Türkiye）
- Private Medinova Hospital
-
-
参加基準
適格基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
サンプリング方法
調査対象母集団
Having undergone coronary artery bypass surgery with median sternotomi
説明
Inclusion Criteria:
- Being over the age of 18
- Having undergone coronary artery bypass surgery (via median sternotomi)
Exclusion Criteria:
- Not having ability to read and write in Turkish
- Having cognitive impairment
- Being in the intensive care unit for more than five days due to medical reasons.
- Having undergone surgery involving thorax or upper extremity in the last 6 months.
- Having neurologic or musculoskeletal problems to prevent evaluation, ambulation and exercise.
- Patients who have an infection or unhealed scar after surgery even if their first measurements are made
研究計画
研究はどのように設計されていますか？
デザインの詳細
- 観測モデル：CASE_ONLY
- 時間の展望：OTHER
この研究は何を測定していますか？
主要な結果の測定
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Change of the Functional Status (with FDQ-s: Turkish version questionnaire)
時間枠：First day at the hospital (pre-op), day of discharge (post-op), 15th day after discharge (control).
|
FDQ-S is a questionnaire created to evaluate the difficulties faced by patients undergoing cardiac surgery, especially when performing functional tasks of the thoracic region and upper extremity. The questionnaire consisting of 10 questions in total, the patients marked how much difficulty they had in each task, on a 100 mm straight line.The first point on the left means "no difficulty" and the last point on the right means "maximum difficulty". The score was determined by measuring from the starting point to the place marked by the patient. The total score is at most 100 points and at least 0 points. The high score indicates that the patient's strain level is high. With time frames we aimed to evaluate the change of the difficulty of patients function. |
First day at the hospital (pre-op), day of discharge (post-op), 15th day after discharge (control).
|
二次結果の測定
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Change of the Mobility Status : (Barthel İndex of Activities of Daily Living)
時間枠：Day of discharge (post-op), 15th day after surgery (control day).
|
Barthel Index determines the level of addiction of the patient in 10 sections: nutrition, washing, self-care, dressing and bowel care, bladder care, toilet care, wheelchair to bed and vice versa, mobility (walking on a smooth surface, using the wheelchair: if appropriate), going up and down stairs.The total score is in the range of 0-100, which means 0-20 points: fully dependent, 21-61: highly dependent, 62-90: moderately dependent, 91-99: slightly dependent, 100 points: fully independent.With time frames we aimed to evaluate the change of the mobility scores. |
Day of discharge (post-op), 15th day after surgery (control day).
|
|
Change of the Quality of Life Status: (SF-36 Quality of Life Questionnaire)
時間枠：Day of discharge (post-op), 15th day after surgery (control day).
|
SF-36 is the most common scale used to measure individuals' quality of life. This scale examines 8 dimensions of health with 36 items such as physical function, role restrictions (due to physical and emotional problems), social function, mental health, vitality (energy), pain and general perception of health.Instead of giving only one total score, the scale gives total score separately for each subscale.100 points indicate good health, 0 points indicate bad health. With time frame we aimed to evaluate the cange of the life quality score of patients. |
Day of discharge (post-op), 15th day after surgery (control day).
|
|
Change of the Pain Status: (Visual Analogue Scale)
時間枠：First day at the hospital (pre-op), day of discharge (post-op), 15th day after surgery (control day).
|
The visual analog scale (VAS) is a validated, subjective measure for acute and chronic pain. Scores are recorded by making a handwritten mark on a 10-cm line that represents a continuum between "no pain" and "worst pain." The distance from the 0 point to the place marked by the patient indicates the pain of the patient. With time frame we aimed to evaluate the change of the life quality score of patients. |
First day at the hospital (pre-op), day of discharge (post-op), 15th day after surgery (control day).
|
|
Change of the Mobility Status: (Perme Intensive Care Mobility Score)
時間枠：Day of discharge (post-op), 15th day after surgery (control day).
|
The Perme ICU Mobility Score is a tool developed to measure the patient's mobility status starting with the ability to follow commands and culminating in the distance walked in two minutes. A total score of 3 or 4 is given for each item, reflecting the patient's mobility. A high score indicates a small amount of mobility barrier and low help, while a low score indicates more mobility and more help needed for mobility. With time frame we aimed to evaluate the change of the mobility score. |
Day of discharge (post-op), 15th day after surgery (control day).
|
その他の成果指標
その他の成果指標
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Age
時間枠：First day at the hospital (pre-op)
|
Age (Year) |
First day at the hospital (pre-op)
|
|
Height
時間枠：First day at the hospital (pre-op)
|
Height in meters |
First day at the hospital (pre-op)
|
|
BMI
時間枠：First day at the hospital
|
BMI (weight and height combined to report BMI in kg/m²) |
First day at the hospital
|
協力者と研究者
協力者
協力者
捜査官
捜査官
- 主任研究者：Ayşe Adıgüzel Bayar, MSc Student、Muğla Sıtkı Koçman University/ Private Medinova Hospital
- スタディディレクター：Baki Umut Tuğay, Prof. Dr.、Muğla Sıtkı Koçman University
研究記録日
主要日程の研究
研究開始 (実際)
研究開始
一次修了 (実際)
一次修了
研究の完了 (実際)
研究の完了
試験登録日
最初に提出
最初に提出
QC基準を満たした最初の提出物
QC基準を満たした最初の提出物
最初の投稿 (実際)
最初の投稿
学習記録の更新
投稿された最後の更新 (実際)
投稿された最後の更新
QC基準を満たした最後の更新が送信されました
QC基準を満たした最後の更新が送信されました
最終確認日
最終確認日
詳しくは
本研究に関する用語
キーワード
その他の研究ID番号
その他の研究ID番号
- MSc Thesis
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
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