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Multimedia-based Hormonal Therapy Information Program for Patients With Prostate Cancer

2021년 3월 3일 업데이트: 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.

연구 개요

상세 설명

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.

연구 유형

중재적

등록 (실제)

80

단계

  • 해당 없음

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 장소

      • Taoyuan, 대만
        • Chang Gung Memorial Hospital at Linkou

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

20년 이상 (성인, 고령자)

건강한 자원 봉사자를 받아들입니다

아니

연구 대상 성별

남성

설명

Inclusion Criteria:

  1. patients with prostate cancer who were receiving hormonal therapy
  2. patients were at least 20 years old
  3. patients were ability to communicate in Chinese or Taiwanese
  4. the married partner agrees to study together, or the single patient has a cohabitation partner who agrees to study together.
  5. patients or family have a smart phone or tablet and can connect to the Internet.

Exclusion Criteria:

  1. having a history of other cancers
  2. unknown diagnosis of prostate cancer or unknown disease status
  3. patients who received chemotherapy, radiotherapy, radical prostatectomy or other treatments for prostate cancer in the past
  4. having history of mental disorder, e.g., phobia, obsessive-compulsive disorder, generalized anxiety, , major depression, mania, manic-depressive psychosis, or dementia
  5. the score of Eastern Cooperative Oncology Group performance is ≧ 2

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 건강 서비스 연구
  • 할당: 무작위
  • 중재 모델: 병렬 할당
  • 마스킹: 하나의

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: Multimedia information group
The experimental group received a weekly multimedia hormone therapy information program for 6 weeks.
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.
간섭 없음: Routine care group
The control group will receive routine care.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Functional Assessment of Cancer Therapy-Prostate (FACT-P)
기간: pretest
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
pretest
Functional Assessment of Cancer Therapy-Prostate (FACT-P)
기간: 8 weeks after the pretest
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
8 weeks after the pretest
Functional Assessment of Cancer Therapy-Prostate (FACT-P)
기간: 12 weeks after the pretest
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
12 weeks after the pretest
The Positive Thinking Scale
기간: pretest
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
pretest
The Positive Thinking Scale
기간: 8 weeks after the pretest
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
8 weeks after the pretest
The Positive Thinking Scale
기간: 12 weeks after the pretest
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
12 weeks after the pretest
The Hormonal Dimension of The Expanded Prostate Cancer Index Composite
기간: pretest
11 items were used, the score of each item ranges from 0 to 100 points. Higher scores indicate fewer hormonal symptoms.
pretest
The Hormonal Dimension of The Expanded Prostate Cancer Index Composite
기간: 8 weeks after the pretest
11 items were used, the score of each item ranges from 0 to 100 points. Higher scores indicate fewer hormonal symptoms.
8 weeks after the pretest
The Hormonal Dimension of The Expanded Prostate Cancer Index Composite
기간: 12 weeks after the pretest
11 items were used, the score of each item ranges from 0 to 100 points. Higher scores indicate fewer hormonal symptoms.
12 weeks after the pretest

2차 결과 측정

결과 측정
측정값 설명
기간
The General Self-Efficacy Scale
기간: pretest
The total scale contains 10 items and a 4-point (1-4) scoring method was adopted. Higher scores indicate higher self-efficacy
pretest
The General Self-Efficacy Scale
기간: 8 weeks after the pretest
The total scale contains 10 items and a 4-point (1-4) scoring method was adopted. Higher scores indicate higher self-efficacy
8 weeks after the pretest
The General Self-Efficacy Scale
기간: 12 weeks after the pretest
The total scale contains 10 items and a 4-point (1-4) scoring method was adopted. Higher scores indicate higher self-efficacy
12 weeks after the pretest
The Social Support Scale
기간: 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.
pretest
The Social Support Scale
기간: 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
The Social Support Scale
기간: 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.
12 weeks after the pretest

기타 결과 측정

결과 측정
측정값 설명
기간
Basic and disease information list 1
기간: pretest
Age
pretest
Basic and disease information list 2
기간: pretest
Education level
pretest
Basic and disease information list 3
기간: pretest
Marital status
pretest
Basic and disease information list 4
기간: pretest
Religion
pretest
Basic and disease information list 5
기간: pretest
Occupation
pretest
Basic and disease information list 6
기간: pretest
Annual family income (NTD)
pretest
Basic and disease information list 7
기간: pretest
Number of children
pretest
Basic and disease information list 8
기간: pretest
Join a support group
pretest
Basic and disease information list 9
기간: pretest
Time since diagnosis (months)
pretest
Basic and disease information list 10
기간: pretest
Tumor-node-metastasis Cancer stage
pretest
Basic and disease information list 11
기간: pretest
Gleason score
pretest
Basic and disease information list 12
기간: pretest
Treatment
pretest
Basic and disease information list 13
기간: pretest
History of chronic disease
pretest
Basic and disease information list 14
기간: pretest
Living status
pretest
Basic and disease information list 15
기간: pretest
Height in centimetre
pretest
Basic and disease information list 16
기간: pretest
Body Mass Index in kg/m2 will be computed from height and body weight
pretest
Basic and disease information list 17
기간: pretest
Body weight in kilograms
pretest
Basic and disease information list 18
기간: pretest
Waist circumference in centimetre
pretest
Basic and disease information list 19
기간: pretest
Serum Prostatic Specific Antigen level
pretest
Basic and disease information list 20
기간: 8 weeks after the pretest
Serum Prostatic Specific Antigen level
8 weeks after the pretest
Basic and disease information list 21
기간: 12 weeks after the pretest
Serum Prostatic Specific Antigen level
12 weeks after the pretest
Basic and disease information list 22
기간: pretest
Perceived health status. A 11-point (0-100) scoring method was used. Higher scores indicate better health condition.
pretest
Basic and disease information list 23
기간: 8 weeks after the pretest
Perceived health status. A 11-point (0-100) scoring method was used. Higher scores indicate better health condition.
8 weeks after the pretest
Basic and disease information list 24
기간: 12 weeks after the pretest
Perceived health status. A 11-point (0-100) scoring method was used. Higher scores indicate better health condition.
12 weeks after the pretest
List of satisfaction with Program
기간: 8 weeks after the pretest
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.
8 weeks after the pretest

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

수사관

  • 수석 연구원: Ching-Hui Chien, PhD, National Taipei University of Nursing and Health Sciences, Taipei city, Taiwan

간행물 및 유용한 링크

연구에 대한 정보 입력을 담당하는 사람이 자발적으로 이러한 간행물을 제공합니다. 이것은 연구와 관련된 모든 것에 관한 것일 수 있습니다.

일반 간행물

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)

2019년 5월 13일

기본 완료 (실제)

2021년 1월 31일

연구 완료 (실제)

2021년 1월 31일

연구 등록 날짜

최초 제출

2020년 12월 23일

QC 기준을 충족하는 최초 제출

2020년 12월 30일

처음 게시됨 (실제)

2021년 1월 5일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2021년 3월 5일

QC 기준을 충족하는 마지막 업데이트 제출

2021년 3월 3일

마지막으로 확인됨

2021년 3월 1일

추가 정보

이 연구와 관련된 용어

개별 참가자 데이터(IPD) 계획

개별 참가자 데이터(IPD)를 공유할 계획입니까?

아니요

IPD 계획 설명

The data of this study will be kept and managed by PI of Ching-Hui Chien.

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

아니

미국 FDA 규제 기기 제품 연구

아니

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

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