Study on the Influence of Forest Therapy on Healing Experience in Botanical Gardens.
2022년 1월 26일 업데이트: Chung-Hua Hsu, Taipei City Hospital
The forest healing system is an important topic of alternative therapy in recent years.
To study the influence of Forest therapy, the establishment of a pilot experimental model system in which both environmental factors and type of activity are necessary.
Therefore, a system based on the Taipei Botanical Garden was introduced by this study.
연구 개요
상세 설명
The forest healing system is an important topic of alternative therapy in recent years.
Forest therapy began in 1989 when the psychology professor Kaplan put forward the "Attention Restoration Theory(ART)".
Awareness has a positive benefit.
To study the influence of Forest therapy, the establishment of a pilot experimental model system in which both environmental factors and type of activity are controlled can greatly reduce the errors caused by the site and the content of the activity.
Therefore, a randomized controlled crossover experiment based on the Taipei Botanical Garden was introduced by this study.
연구 유형
중재적
등록 (실제)
42
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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Taipei, 대만, 10845
- Taipei City Hospital
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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
공부할 수 있는 나이
20년 (성인)
건강한 자원 봉사자를 받아들입니다
아니
연구 대상 성별
모두
설명
Inclusion Criteria:
- 20-35 years old youth (not limited to men and women)
- Those who have the ability and physical strength to walk for more than 120 minutes
- Subjects must voluntarily join the study
Exclusion Criteria:
- People who smoke or chew betel nuts
- People who have the habit of drinking (drinking more than five standard glasses in any situation)
- Drug addiction (including narcotic drugs and non-narcotics) habitual
- Those who have taken psychosomatic drugs in the past 30 days
- Participating in another clinical trial at the same time, or in the follow-up period of an interventional trial
- Those diagnosed with major injuries
- Women who are currently pregnant or breastfeeding
- Conditions where other subjects cannot cooperate (for example: unable to participate after random assignment, and not signing the subject's consent form)
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: 크로스오버 할당
- 마스킹: 없음(오픈 라벨)
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
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실험적: activities in the Botanical Garden or Urban
experiment group is activities in the Botanical Garden, and the control group is activities in urban
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activities in the Taipei Botanical Garden or in Urban
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다른: Cross-over design
The participants are randomized divided into in two groups following by the experiment which is designed by two consecutive times at one week intervals, and the experimental activities and the control activities are staggered.
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activities in the Taipei Botanical Garden or in Urban
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연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
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questionnaire: BPOMS (1st)
기간: baseline, pre-intervention(1st) → 2 hours intervention → immediately after the intervention(1st)
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Change from baseline Brief Profile of Mood States at first intervention
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baseline, pre-intervention(1st) → 2 hours intervention → immediately after the intervention(1st)
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questionnaire: BPOMS (2nd)
기간: pre-intervention(2nd) → 2 hours intervention → immediately after the intervention(2nd)
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Change from Brief Profile of Mood States at second intervention after 7-day-washout period & cross-over
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pre-intervention(2nd) → 2 hours intervention → immediately after the intervention(2nd)
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questionnaire: BAI (1st)
기간: baseline, pre-intervention(1st) → 2 hours intervention → immediately after the intervention(1st)
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Change from baseline The Beck Anxiety Inventory at first intervention
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baseline, pre-intervention(1st) → 2 hours intervention → immediately after the intervention(1st)
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questionnaire: BAI (2nd)
기간: pre-intervention(2nd) → 2 hours intervention → immediately after the intervention(2nd)
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Change from The Beck Anxiety Inventory at second intervention after 7-day-washout
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pre-intervention(2nd) → 2 hours intervention → immediately after the intervention(2nd)
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questionnaire: BDI-II (1st)
기간: baseline, pre-intervention(1st) → 2 hours intervention → immediately after the intervention(1st)
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Change from baseline The Beck Depression Inventory II at first intervention
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baseline, pre-intervention(1st) → 2 hours intervention → immediately after the intervention(1st)
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questionnaire: BDI-II (2nd)
기간: pre-intervention(2nd) → 2 hours intervention → immediately after the intervention(2nd)
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Change from The Beck Depression Inventory II at second intervention after 7-day-washout
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pre-intervention(2nd) → 2 hours intervention → immediately after the intervention(2nd)
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questionnaire: BSRS-V (1st)
기간: baseline, pre-intervention(1st) → 2 hours intervention → immediately after the intervention(1st)
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Change from baseline Brief Symptom Rating Scale V at first intervention
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baseline, pre-intervention(1st) → 2 hours intervention → immediately after the intervention(1st)
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questionnaire: BSRS-V (2nd)
기간: pre-intervention(2nd) → 2 hours intervention → immediately after the intervention(2nd)
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Change from Brief Symptom Rating Scale V at second intervention after 7-day-washout
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pre-intervention(2nd) → 2 hours intervention → immediately after the intervention(2nd)
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physiological indicator: alpha-amylase activity in salivary (1st)
기간: baseline, pre-intervention(1st) → 2 hours intervention → immediately after the intervention(1st)
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Change from baseline alpha-amylase activity in salivary by using commercial kits (Salimetrics®) at first intervention
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baseline, pre-intervention(1st) → 2 hours intervention → immediately after the intervention(1st)
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physiological indicator: alpha-amylase activity in salivary (2nd)
기간: pre-intervention(2nd) → 2 hours intervention → immediately after the intervention(2nd)
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Change from alpha-amylase activity in salivary by using commercial kits (Salimetrics®) at second intervention after 7-day-washout
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pre-intervention(2nd) → 2 hours intervention → immediately after the intervention(2nd)
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physiological indicator: HRV (Heart Rate Variability) (1st)
기간: baseline, pre-intervention(1st) → 2 hours intervention → immediately after the intervention(1st)
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Change from baseline HRV by using wrist monitors (ANSWatch®) to measure heart rate, heart rate variability (related to activities of the autonomic nervous system ANS), irregular heartbeats (IRRHB), and 5-minute continuous pulse wave at first intervention
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baseline, pre-intervention(1st) → 2 hours intervention → immediately after the intervention(1st)
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physiological indicator: HRV (Heart Rate Variability) (2nd)
기간: pre-intervention(2nd) → 2 hours intervention → immediately after the intervention(2nd)
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Change from HRV by using wrist monitors (ANSWatch®) to measure heart rate, heart rate variability (related to activities of the autonomic nervous system ANS), irregular heartbeats (IRRHB), and 5-minute continuous pulse wave at second intervention after 7-day-washout
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pre-intervention(2nd) → 2 hours intervention → immediately after the intervention(2nd)
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physiological indicator: blood pressures (systolic and diastolic) (1st)
기간: baseline, pre-intervention(1st) → 2 hours intervention → immediately after the intervention(1st)
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Change from baseline blood pressures by using wrist monitors (ANSWatch®) to measure blood pressures (systolic and diastolic) at first intervention
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baseline, pre-intervention(1st) → 2 hours intervention → immediately after the intervention(1st)
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physiological indicator: blood pressures (systolic and diastolic) (2nd)
기간: pre-intervention(2nd) → 2 hours intervention → immediately after the intervention(2nd)
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Change from blood pressures by using wrist monitors (ANSWatch®) to measure blood pressures (systolic and diastolic) at second intervention after 7-day-washout
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pre-intervention(2nd) → 2 hours intervention → immediately after the intervention(2nd)
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공동 작업자 및 조사자
여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.
수사관
- 연구 책임자: Chung-Hua Hsu, Branch of Chinese Medicine, Taipei City Hospital
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)
2021년 4월 27일
기본 완료 (실제)
2021년 4월 27일
연구 완료 (실제)
2021년 10월 26일
연구 등록 날짜
최초 제출
2021년 12월 8일
QC 기준을 충족하는 최초 제출
2022년 1월 26일
처음 게시됨 (실제)
2022년 2월 8일
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
2022년 2월 8일
QC 기준을 충족하는 마지막 업데이트 제출
2022년 1월 26일
마지막으로 확인됨
2022년 1월 1일
추가 정보
이 연구와 관련된 용어
키워드
기타 연구 ID 번호
- TCHIRB-11002014
약물 및 장치 정보, 연구 문서
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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. .