Multimedia-based Hormonal Therapy Information Program for Patients With Prostate Cancer
2021年3月3日 更新者：Ching-Hui Chien、National Taipei University of Nursing and Health Sciences
Development and Evaluation of the Effectiveness of a Multimedia-based Hormonal Therapy Information Program for Patients With Prostate Cancer
This study takes place in the Divisions of Urology.
Patients who have only received hormonal therapy will be enrolled.
Patients will be randomly sorted into an experimental group and a control group after completing a pretest questionnaire.
The experimental group will receive the the multimedia hormone therapy information program once per week for 6 consecutive weeks, while the control group will receive routine care.
The follow-up data collections will be completed at 8 and 12 weeks after the pretest.
For quantitative measurement, the main variables will be social support, self-efficacy, quality of life, and positive thinking.
調査の概要
詳細な説明
This study takes place in the Divisions of Urology at Chang Gung Memorial Hospitals.
Patients who have only received hormonal therapy will be enrolled.
With reference to past research findings, self-efficacy theory, and experts' advice, a multimedia hormone therapy information program was developed.
The multimedia hormone therapy information program covered 6 topics, namely the recognition of hormone therapy and multimedia information programs, mindfulness, exercise, stress relief, positive thinking, and prevention or reduction of fatigue.
A pilot study will be conducted to check the feasibility of intervention study design and the effectiveness of the program will be tested.
Patients will be randomly sorted into an experimental group (multimedia information group, n = 36 to 40) and a control group (routine care group, n = 36 to 40) after completing a pretest questionnaire.
The experimental group will receive the multimedia information intervention once per week for 6 consecutive weeks, while the control group will receive routine care.
The follow-up data collections will be completed at 8 and 12 weeks after the pretest.
For quantitative measurement, the main variables will be social support, self-efficacy, quality of life, positive thinking, and satisfaction with program.
Generalized Estimating Equations (GEEs) will be used to o analyze data.
研究の種類
介入
入学 (実際)
80
段階
- 適用できない
連絡先と場所
このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。
研究場所
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Taoyuan、台湾
- Chang Gung Memorial Hospital at Linkou
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参加基準
研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。
適格基準
就学可能な年齢
20年歳以上 (大人、高齢者)
健康ボランティアの受け入れ
いいえ
受講資格のある性別
男
説明
Inclusion Criteria:
- patients with prostate cancer who were receiving hormonal therapy
- patients were at least 20 years old
- patients were ability to communicate in Chinese or Taiwanese
- the married partner agrees to study together, or the single patient has a cohabitation partner who agrees to study together.
- patients or family have a smart phone or tablet and can connect to the Internet.
Exclusion Criteria:
- having a history of other cancers
- unknown diagnosis of prostate cancer or unknown disease status
- patients who received chemotherapy, radiotherapy, radical prostatectomy or other treatments for prostate cancer in the past
- having history of mental disorder, e.g., phobia, obsessive-compulsive disorder, generalized anxiety, , major depression, mania, manic-depressive psychosis, or dementia
- the score of Eastern Cooperative Oncology Group performance is ≧ 2
研究計画
このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。
研究はどのように設計されていますか？
デザインの詳細
- 主な目的：ヘルスサービス研究
- 割り当て：ランダム化
- 介入モデル：並列代入
- マスキング：独身
武器と介入
参加者グループ / アーム |
介入・治療 |
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実験的：Multimedia information group
The experimental group received a weekly multimedia hormone therapy information program for 6 weeks.
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The multimedia hormone therapy information program lasted 6 weeks and covered 6 topics, namely the recognition of hormone therapy and multimedia information programs, mindfulness, exercise, stress relief, positive thinking, and prevention or reduction of fatigue.
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介入なし：Routine care group
The control group will receive routine care.
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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 |
|---|---|---|
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Functional Assessment of Cancer Therapy-Prostate (FACT-P)
時間枠：pretest
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A total of 39 items, including five subdimensions, namely, physical well-being, social/family well-being, emotional well-being, functional well-being, and prostate cancer subscales.
A 5-point scoring method was adopted.
Higher scores indicate higher quality of life
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pretest
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Functional Assessment of Cancer Therapy-Prostate (FACT-P)
時間枠：8 weeks after the pretest
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A total of 39 items, including five subdimensions, namely, physical well-being, social/family well-being, emotional well-being, functional well-being, and prostate cancer subscales.
A 5-point scoring method was adopted.
Higher scores indicate higher quality of life
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8 weeks after the pretest
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Functional Assessment of Cancer Therapy-Prostate (FACT-P)
時間枠：12 weeks after the pretest
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A total of 39 items, including five subdimensions, namely, physical well-being, social/family well-being, emotional well-being, functional well-being, and prostate cancer subscales.
A 5-point scoring method was adopted.
Higher scores indicate higher quality of life
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12 weeks after the pretest
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The Positive Thinking Scale
時間枠：pretest
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A total of 18 items, including two subscales of personal satisfaction and goal pursuit.
A five-point (1-5) scoring method was used.
Higher scores indicate a higher level of positive thinking
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pretest
|
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The Positive Thinking Scale
時間枠：8 weeks after the pretest
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A total of 18 items, including two subscales of personal satisfaction and goal pursuit.
A five-point (1-5) scoring method was used.
Higher scores indicate a higher level of positive thinking
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8 weeks after the pretest
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The Positive Thinking Scale
時間枠：12 weeks after the pretest
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A total of 18 items, including two subscales of personal satisfaction and goal pursuit.
A five-point (1-5) scoring method was used.
Higher scores indicate a higher level of positive thinking
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12 weeks after the pretest
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The Hormonal Dimension of The Expanded Prostate Cancer Index Composite
時間枠：pretest
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11 items were used, the score of each item ranges from 0 to 100 points.
Higher scores indicate fewer hormonal symptoms.
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pretest
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The Hormonal Dimension of The Expanded Prostate Cancer Index Composite
時間枠：8 weeks after the pretest
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11 items were used, the score of each item ranges from 0 to 100 points.
Higher scores indicate fewer hormonal symptoms.
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8 weeks after the pretest
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The Hormonal Dimension of The Expanded Prostate Cancer Index Composite
時間枠：12 weeks after the pretest
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11 items were used, the score of each item ranges from 0 to 100 points.
Higher scores indicate fewer hormonal symptoms.
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12 weeks after the pretest
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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The General Self-Efficacy Scale
時間枠：pretest
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The total scale contains 10 items and a 4-point (1-4) scoring method was adopted.
Higher scores indicate higher self-efficacy
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pretest
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The General Self-Efficacy Scale
時間枠：8 weeks after the pretest
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The total scale contains 10 items and a 4-point (1-4) scoring method was adopted.
Higher scores indicate higher self-efficacy
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8 weeks after the pretest
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The General Self-Efficacy Scale
時間枠：12 weeks after the pretest
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The total scale contains 10 items and a 4-point (1-4) scoring method was adopted.
Higher scores indicate higher self-efficacy
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12 weeks after the pretest
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The Social Support Scale
時間枠：pretest
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A total of 16 items, including four sub-scales of emotional, informational, appraisal, and instrumental support.
A 4-point scoring method (0-3) was used.
Higher scores indicate stronger support.
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pretest
|
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The Social Support Scale
時間枠：8 weeks after the pretest
|
A total of 16 items, including four sub-scales of emotional, informational, appraisal, and instrumental support.
A 4-point scoring method (0-3) was used.
Higher scores indicate stronger support.
|
8 weeks after the pretest
|
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The Social Support Scale
時間枠：12 weeks after the pretest
|
A total of 16 items, including four sub-scales of emotional, informational, appraisal, and instrumental support.
A 4-point scoring method (0-3) was used.
Higher scores indicate stronger support.
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12 weeks after the pretest
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その他の成果指標
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Basic and disease information list 1
時間枠：pretest
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Age
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pretest
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Basic and disease information list 2
時間枠：pretest
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Education level
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pretest
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Basic and disease information list 3
時間枠：pretest
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Marital status
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pretest
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Basic and disease information list 4
時間枠：pretest
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Religion
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pretest
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Basic and disease information list 5
時間枠：pretest
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Occupation
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pretest
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Basic and disease information list 6
時間枠：pretest
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Annual family income (NTD)
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pretest
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Basic and disease information list 7
時間枠：pretest
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Number of children
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pretest
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Basic and disease information list 8
時間枠：pretest
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Join a support group
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pretest
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Basic and disease information list 9
時間枠：pretest
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Time since diagnosis (months)
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pretest
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Basic and disease information list 10
時間枠：pretest
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Tumor-node-metastasis Cancer stage
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pretest
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Basic and disease information list 11
時間枠：pretest
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Gleason score
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pretest
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Basic and disease information list 12
時間枠：pretest
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Treatment
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pretest
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Basic and disease information list 13
時間枠：pretest
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History of chronic disease
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pretest
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Basic and disease information list 14
時間枠：pretest
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Living status
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pretest
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Basic and disease information list 15
時間枠：pretest
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Height in centimetre
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pretest
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Basic and disease information list 16
時間枠：pretest
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Body Mass Index in kg/m2 will be computed from height and body weight
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pretest
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Basic and disease information list 17
時間枠：pretest
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Body weight in kilograms
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pretest
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Basic and disease information list 18
時間枠：pretest
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Waist circumference in centimetre
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pretest
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Basic and disease information list 19
時間枠：pretest
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Serum Prostatic Specific Antigen level
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pretest
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Basic and disease information list 20
時間枠：8 weeks after the pretest
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Serum Prostatic Specific Antigen level
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8 weeks after the pretest
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Basic and disease information list 21
時間枠：12 weeks after the pretest
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Serum Prostatic Specific Antigen level
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12 weeks after the pretest
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Basic and disease information list 22
時間枠：pretest
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Perceived health status.
A 11-point (0-100) scoring method was used.
Higher scores indicate better health condition.
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pretest
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Basic and disease information list 23
時間枠：8 weeks after the pretest
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Perceived health status.
A 11-point (0-100) scoring method was used.
Higher scores indicate better health condition.
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8 weeks after the pretest
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Basic and disease information list 24
時間枠：12 weeks after the pretest
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Perceived health status.
A 11-point (0-100) scoring method was used.
Higher scores indicate better health condition.
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12 weeks after the pretest
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List of satisfaction with Program
時間枠：8 weeks after the pretest
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Five items were self-designed to understand the satisfaction of men in the experimental group.
A 11-point (0-100) scoring method was used.
Higher scores indicate higher satisfaction.
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8 weeks after the pretest
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協力者と研究者
ここでは、この調査に関係する人々や組織を見つけることができます。
捜査官
- 主任研究者：Ching-Hui Chien, PhD、National Taipei University of Nursing and Health Sciences, Taipei city, Taiwan
出版物と役立つリンク
研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。
一般刊行物
- Cella DF, Tulsky DS, Gray G, Sarafian B, Linn E, Bonomi A, Silberman M, Yellen SB, Winicour P, Brannon J, et al. The Functional Assessment of Cancer Therapy scale: development and validation of the general measure. J Clin Oncol. 1993 Mar;11(3):570-9. doi: 10.1200/JCO.1993.11.3.570.
- Wei JT, Dunn RL, Litwin MS, Sandler HM, Sanda MG. Development and validation of the expanded prostate cancer index composite (EPIC) for comprehensive assessment of health-related quality of life in men with prostate cancer. Urology. 2000 Dec 20;56(6):899-905. doi: 10.1016/s0090-4295(00)00858-x.
- Esper P, Mo F, Chodak G, Sinner M, Cella D, Pienta KJ. Measuring quality of life in men with prostate cancer using the functional assessment of cancer therapy-prostate instrument. Urology. 1997 Dec;50(6):920-8. doi: 10.1016/S0090-4295(97)00459-7.
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- Diefenbach MA, Mohamed NE, Butz BP, Bar-Chama N, Stock R, Cesaretti J, Hassan W, Samadi D, Hall SJ. Acceptability and preliminary feasibility of an internet/CD-ROM-based education and decision program for early-stage prostate cancer patients: randomized pilot study. J Med Internet Res. 2012 Jan 13;14(1):e6. doi: 10.2196/jmir.1891.
- Global Burden of Disease Cancer Collaboration; Fitzmaurice C, Akinyemiju TF, Al Lami FH, Alam T, Alizadeh-Navaei R, Allen C, Alsharif U, Alvis-Guzman N, Amini E, Anderson BO, Aremu O, Artaman A, Asgedom SW, Assadi R, Atey TM, Avila-Burgos L, Awasthi A, Ba Saleem HO, Barac A, Bennett JR, Bensenor IM, Bhakta N, Brenner H, Cahuana-Hurtado L, Castaneda-Orjuela CA, Catala-Lopez F, Choi JJ, Christopher DJ, Chung SC, Curado MP, Dandona L, Dandona R, das Neves J, Dey S, Dharmaratne SD, Doku DT, Driscoll TR, Dubey M, Ebrahimi H, Edessa D, El-Khatib Z, Endries AY, Fischer F, Force LM, Foreman KJ, Gebrehiwot SW, Gopalani SV, Grosso G, Gupta R, Gyawali B, Hamadeh RR, Hamidi S, Harvey J, Hassen HY, Hay RJ, Hay SI, Heibati B, Hiluf MK, Horita N, Hosgood HD, Ilesanmi OS, Innos K, Islami F, Jakovljevic MB, Johnson SC, Jonas JB, Kasaeian A, Kassa TD, Khader YS, Khan EA, Khan G, Khang YH, Khosravi MH, Khubchandani J, Kopec JA, Kumar GA, Kutz M, Lad DP, Lafranconi A, Lan Q, Legesse Y, Leigh J, Linn S, Lunevicius R, Majeed A, Malekzadeh R, Malta DC, Mantovani LG, McMahon BJ, Meier T, Melaku YA, Melku M, Memiah P, Mendoza W, Meretoja TJ, Mezgebe HB, Miller TR, Mohammed S, Mokdad AH, Moosazadeh M, Moraga P, Mousavi SM, Nangia V, Nguyen CT, Nong VM, Ogbo FA, Olagunju AT, Pa M, Park EK, Patel T, Pereira DM, Pishgar F, Postma MJ, Pourmalek F, Qorbani M, Rafay A, Rawaf S, Rawaf DL, Roshandel G, Safiri S, Salimzadeh H, Sanabria JR, Santric Milicevic MM, Sartorius B, Satpathy M, Sepanlou SG, Shackelford KA, Shaikh MA, Sharif-Alhoseini M, She J, Shin MJ, Shiue I, Shrime MG, Sinke AH, Sisay M, Sligar A, Sufiyan MB, Sykes BL, Tabares-Seisdedos R, Tessema GA, Topor-Madry R, Tran TT, Tran BX, Ukwaja KN, Vlassov VV, Vollset SE, Weiderpass E, Williams HC, Yimer NB, Yonemoto N, Younis MZ, Murray CJL, Naghavi M. Global, Regional, and National Cancer Incidence, Mortality, Years of Life Lost, Years Lived With Disability, and Disability-Adjusted Life-Years for 29 Cancer Groups, 1990 to 2016: A Systematic Analysis for the Global Burden of Disease Study. JAMA Oncol. 2018 Nov 1;4(11):1553-1568. doi: 10.1001/jamaoncol.2018.2706.
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研究記録日
これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。
主要日程の研究
研究開始 (実際)
2019年5月13日
一次修了 (実際)
2021年1月31日
研究の完了 (実際)
2021年1月31日
試験登録日
最初に提出
2020年12月23日
QC基準を満たした最初の提出物
2020年12月30日
最初の投稿 (実際)
2021年1月5日
学習記録の更新
投稿された最後の更新 (実際)
2021年3月5日
QC基準を満たした最後の更新が送信されました
2021年3月3日
最終確認日
2021年3月1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
- 201602024B0C501
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?
いいえ
IPD プランの説明
The data of this study will be kept and managed by PI of Ching-Hui Chien.
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
いいえ
米国FDA規制機器製品の研究
いいえ
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。