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Clinical Trials/NCT03304301
NCT03304301UnknownNot Applicable

Effect of Sunlight Exposure and Outdoor Activities on Improving the Depression, Cognition and Quality of Life of the Institutionalized Elderly: A Randomized Controlled Trial

Chiayi Christian Hospital1 site in 1 country74 target enrollmentStarted: June 30, 2016Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Sponsor
Enrollment
74
Locations
1
Primary Endpoint
Change from baseline depression at 3 months

Study Overview

Brief Summary

Background: The transition to long-term care facility can be a stressful and emotional event for the elderly. The evidences showed that the prevalence of depression and the cognition impairment were higher in the institutionalized elderly than the community dwelling elderly. It could affect the quality of life of the elderly and increase risk of mortality.

Purpose: The aim of the study is to evaluate the effect of outdoor activities and sunlight exposure on depression, cognitive function, and quality of life among institutionalized elderly.

Method: The design is a randomized control trial. Participants will be randomly allocated to experimental or control groups by block randomization. In the experimental group, participants will be encouraged to reduce time spent on bed and bedroom. Nurses, nurse aids or family will take participants outdoors and exposure their face, hands or arm to sunlight for 15-30 minutes a day, five days a week for three months (if the UV index is over 8 according to the forecast of Center Weather Bureau, the participants will be asked to stay inside). In the control group, the participants will receive routine care. The control group will neither be encouraged to stay outdoors nor limit the chance to exposure to sunlight.

Expected outcome: The expected benefit of the research is to improve the depression, cognitive function, and quality of life of the institutionalized elderly.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
65 Years to — (Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •resident in the long-term care facility for at least 6 months
  • •Barthel Index score is equal or over 20
  • •able to communicate
  • •life expectancy over 12 months
  • •conscious clear

Exclusion Criteria

  • •allergy to sunlight
  • •diagnosed with skin cancer

Arms & Interventions

experimental group

Experimental

Participants will be encouraged to reduce time spent on bed and bedroom. We will also take participants outdoors and expose to sunlight (if the UV index is over 8 according to the forecast of Center Weather Bureau, the participants will be asked to stay inside) five days a week for three months.

Intervention: sunlight exposure (Behavioral)

control group

No Intervention

Participants will receive routine care.

Outcomes

Primary Outcomes

Change from baseline depression at 3 months

Time Frame: baseline, three month after recruitment

measured with GDS-15

Secondary Outcomes

  • Change from baseline cognitive function at 3 months(baseline, three month after recruitment)

Investigators

Sponsor
Chiayi Christian Hospital
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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