Characteristics and Medical Resource Utilization of Postoperative Patients
Characteristics and Medical Resource Utilization of Postoperative Patients: A Cross-sectional Survey of Outpatients
調査の概要
状態
条件
詳細な説明
A considerable number of patients suffer prolonged chronic pain that does not retract or diminish after surgery, and are thus unable to achieve the desired results in receiving surgical treatment. Postoperative pain is gradually being perceived as a social issue as opposed to a personal health condition. Meanwhile, although efforts to address chronic pain with integrative medicine are continued in answer to the lack of success of pain management through surgery, there is still a lack of supporting evidence.
The objective of this survey study is to assess the characteristics, usage of conventional and Korean medical services, and prognosis by period before and after surgery in postoperative patients visiting a Korean medicine hospital, and analyze the associations between the preference for conventional and Korean medicine treatment. This study therefore investigates the usage of conventional and Korean medical services in postoperative patients, and is expected to provide information that will potentially aid patient decision making.
研究の種類
入学 (実際)
連絡先と場所
研究場所
-
-
-
Seoul、大韓民国
- Jaseng Medical Foundation
-
-
参加基準
適格基準
就学可能な年齢
- 子
- 大人
- 高齢者
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
説明
Inclusion Criteria:
- Patients with chief complaint(s) of at least one or more of the following: low back pain (or radiating leg pain), neck pain (or radiating arm pain), knee pain, or shoulder pain
- Patients with a history of musculoskeletal surgery related to the chief complaint(s)
- Patients capable of effective communication with the researcher(s) and understanding the survey items
- Patients who have given written informed consent
Exclusion Criteria:
- Patients without a history of musculoskeletal surgery associated with the low back, neck, shoulder, or knee region(s)
- Patients whose current pain is mainly attributed to traffic accident injury
- Patients incapable of answering the researcher interviews and surveys
- Patients with other reasons rendering study participation inappropriate as judged by the researcher(s)
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
この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
---|---|---|
Numeric rating scale (NRS) of pain
時間枠:Within 7 days after 1st visit
|
11-point pain scale
|
Within 7 days after 1st visit
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
---|---|---|
Five level version of EuroQol-5 Dimension (EQ-5D-5L)
時間枠:Within 7 days after 1st visit
|
Health-related quality of life questionnaire consisting of 5 descriptive items and EQ Visual Analogue Scales (EQ-VASs)
|
Within 7 days after 1st visit
|
Functional disability questionnaire (for low back pain patients as indicated by postoperative condition)
時間枠:Within 7 days after 1st visit
|
Oswestry Disability Index (ODI)
|
Within 7 days after 1st visit
|
Functional disability questionnaire (for neck pain patients as indicated by postoperative condition)
時間枠:Within 7 days after 1st visit
|
Neck Disability Index (NDI)
|
Within 7 days after 1st visit
|
Functional disability questionnaire (for knee pain patients as indicated by postoperative condition)
時間枠:Within 7 days after 1st visit
|
Western Ontario McMaster Universities Osteoarthritis Index (WOMAC)
|
Within 7 days after 1st visit
|
Functional disability questionnaire (for shoulder pain patients as indicated by postoperative condition)
時間枠:Within 7 days after 1st visit
|
Shoulder Pain and Disability Index (SPADI)
|
Within 7 days after 1st visit
|
Work Productivity and Activity Impairment Questionnaire: General Health (WPAI-GH)
時間枠:Within 7 days after 1st visit
|
Questionnaire assessing the effect of health problems on the ability to work and to perform regular activities
|
Within 7 days after 1st visit
|
Beck Depression Inventory-II (BDI-II)
時間枠:Within 7 days after 1st visit
|
The Korean version of the BDI-II has been validated and consists of 21 multiple choice items for diagnosis of depression.
|
Within 7 days after 1st visit
|
Medical service use
時間枠:Within 7 days after 1st visit
|
Type(s) of medical service use before and after surgery post-onset
|
Within 7 days after 1st visit
|
Medical costs
時間枠:Within 7 days after 1st visit
|
Medical costs from medical service use before and after surgery post-onset
|
Within 7 days after 1st visit
|
Satisfaction with and preference for conventional and Korean medicine
時間枠:Within 7 days after 1st visit
|
Satisfaction with and preference for conventional and Korean medicine as measured using a 9-point Likert scale
|
Within 7 days after 1st visit
|
協力者と研究者
捜査官
- 主任研究者:In-Hyuk Ha, KMD, M.Sc.、Jaseng Medical Foundation
研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (実際)
研究の完了 (実際)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
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
詳しくは
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。
痛み、術後の臨床試験
-
Dexa Medica Group完了