CompletedNot Applicable

Study on the Influence of Forest Therapy on Healing Experience in Botanical Gardens.

Taiwan42 participantsStarted 2021-04-27

Plain-language summary

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.

Who can participate

Age range20 Years – 35 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

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)

What they're measuring

questionnaire: BPOMS (1st)

Timeframe: baseline, pre-intervention(1st) → 2 hours intervention → immediately after the intervention(1st)

questionnaire: BPOMS (2nd)

Timeframe: pre-intervention(2nd) → 2 hours intervention → immediately after the intervention(2nd)

questionnaire: BAI (1st)

Timeframe: baseline, pre-intervention(1st) → 2 hours intervention → immediately after the intervention(1st)

questionnaire: BAI (2nd)

Timeframe: pre-intervention(2nd) → 2 hours intervention → immediately after the intervention(2nd)

questionnaire: BDI-II (1st)

Timeframe: baseline, pre-intervention(1st) → 2 hours intervention → immediately after the intervention(1st)

questionnaire: BDI-II (2nd)

Timeframe: pre-intervention(2nd) → 2 hours intervention → immediately after the intervention(2nd)

questionnaire: BSRS-V (1st)

Timeframe: baseline, pre-intervention(1st) → 2 hours intervention → immediately after the intervention(1st)

Trial details

NCT IDNCT05228704

SponsorTaipei City Hospital

Sponsor typeOTHER_GOV

Study typeINTERVENTIONAL

Primary completion2021-04-27

View on ClinicalTrials.gov More Nature, Human trials

Plain-language summary

Who can participate

Age range20 Years – 35 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

What they're measuring

questionnaire: BPOMS (1st)

Timeframe: baseline, pre-intervention(1st) → 2 hours intervention → immediately after the intervention(1st)

questionnaire: BPOMS (2nd)

Timeframe: pre-intervention(2nd) → 2 hours intervention → immediately after the intervention(2nd)

questionnaire: BAI (1st)

Timeframe: baseline, pre-intervention(1st) → 2 hours intervention → immediately after the intervention(1st)

questionnaire: BAI (2nd)

Timeframe: pre-intervention(2nd) → 2 hours intervention → immediately after the intervention(2nd)

questionnaire: BDI-II (1st)

Timeframe: baseline, pre-intervention(1st) → 2 hours intervention → immediately after the intervention(1st)

questionnaire: BDI-II (2nd)

Timeframe: pre-intervention(2nd) → 2 hours intervention → immediately after the intervention(2nd)

questionnaire: BSRS-V (1st)

Timeframe: baseline, pre-intervention(1st) → 2 hours intervention → immediately after the intervention(1st)