Development of forest healing rehabilitation program and verification of effects on the physically weak.

Development of forest healing rehabilitation program and verification of physical, physiological and psychological effects on the physically weak.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0007249

Enrollment

Registered

2022-05-06

Start date

2022-05-12

Completion date

Unknown

Last updated

2023-06-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Others : The forest healing rehabilitation program, which is an intervention method of the study, is implemented at the National Recreational Forest in Korea. The study subjects assemble and disband a

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Among the patients who visited International St. Mary's Hospital and the elderly 65 years or older who expressed their intention to participate in this clinical study through advertisements inside and outside the hospital, those who satisfy one or more of the following items are selected. 1) Those with a history of stroke 2) Those who complain of subjective cognitive impairment 3) Those who complain of subjective physical function deterioration 4) Gait function is a factor of 4 FAC (supervision gait)

Exclusion criteria

Exclusion criteria: 1) Patients who show symptoms or signs of heart, peripheral blood vessel, and cerebrovascular disease according to the ACSM guide - pain or discomfort in the chest, neck, jaw, arms, or other areas that may be due to cardiac ischemia; - During rest or light exercise dyspnea / dizziness or fainting / shortness of breath or paroxysmal nocturnal dyspnea / swelling of the ankles / palpitations or tachycardia; - History of heart murmur (murmur) - Unusual fatigue or shortness of breath when performing usual activities 2) Those who cannot walk independently without assistance (orthosis, cane, etc.) or help from others. (FAC <4) 3) Those who have moderate or more cognitive impairment (less than 20 MMSE points) or are illiterate 4) Those with underlying diseases that require attention related to exercise (asthma, chronic obstructive pulmonary disease, heart disease, anemia, brain tumor, hypotension) 5) Those who are undergoing medical treatment that may cause deterioration of physical function (radiotherapy, chemotherapy) 6) Those who are participating in other clinical research 7) Those who did not agree to participate in the study

Design outcomes

Primary

Measure	Time frame
Balance;Aerobic capacity ;Walking;Breathing;Flexibility;Physical activity ;Blood pressure;Pulse rate;Weight;Waist circumference; Cognitive function;Affective function (Depression, Anxiety, Perceived Stress);Quality of Life	—

Secondary

Measure	Time frame
Subgroup analysis (Stroke, mild cognitive impairment) ;Compared study (Group did or did not complete the program)	—

Countries

Korea, Republic of

Contacts

Public ContactHawon Lim

Catholic Kwandong University International St.Mary's Hospital

hwon1617@gmail.com+82-32-290-3096

Outcome results