Development of forest healing rehabilitation program and verification of effects on the physically weak.
- Conditions
- Diseases of the circulatory system
- Registration Number
- KCT0007249
- Lead Sponsor
- Catholic Kwandong University International St.Mary's Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 40
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)
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
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 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 Outcome Measures
Name Time Method Subgroup analysis (Stroke, mild cognitive impairment) ;Compared study (Group did or did not complete the program)