Pre-frail Elderly Clinical Trial
Official title:
The Effect of Superoxide Dismutase (SOD) Enzyme on Frailty and Health Related Quality of Life Among Indonesian Pre-frail Elderly: A Double Blind Randomized Controlled Trial
The primary objective is to determine the effect of SOD enzyme on frailty and health related
quality of life among Indonesian pre-frail elderly.
The secondary objective is to determine the effect of SOD enzyme on anti-oxidant status,
morbidity, and hospitalization among Indonesian pre-frail elderly.
The study hypothesis:
1. SOD enzyme can improve frailty status and health related quality of life among
Indonesian pre-frail elderly.
2. SOD enzyme can increase anti-oxidant serum status among Indonesian pre-frail elderly.
3. SOD enzyme can decrease morbidity among Indonesian pre-frail elderly.
4. SOD enzyme can decrease hospitalization events among Indonesian pre-frail elderly.
Status | Recruiting |
Enrollment | 150 |
Est. completion date | April 2017 |
Est. primary completion date | February 2017 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 60 Years and older |
Eligibility |
Inclusion Criteria: - Elderly aged 60 years or more with pre-frail condition - Patients with SOD enzyme deficiency - Willing to participate Exclusion Criteria: - Patients with cognitive function impairment (AMT score < 8) - Patients with depression (Geriatric depression scale score >= 10) - Patients with history of cirrhotic hepatic disease or severe hepatic disease - Patients with kidney function impairment - Patients with gluten allergy and derivative products - Patients consume other antioxidant and omega-3 supplement |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Indonesia | Cipto Mangunkusumo National Hospital | Jakarta |
Lead Sponsor | Collaborator |
---|---|
Indonesia University |
Indonesia,
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* Note: There are 17 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Frailty status | Measured by FI-40 item questionnaire. | 6 months (24 weeks) | No |
Secondary | Health related quality of life | Measured by EQ5D questionnaire. | 6 months (24 weeks) | No |
Secondary | Anti-oxidant serum status | Measured by erythrocyte antioxidant enzymes activity, i.e. superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPX). | 6 months (24 weeks) | No |
Secondary | Morbidity | Measured by Cumulative Illness Rating Score (CIRS). | 6 months (24 weeks) | No |
Secondary | Hospitalization | Observed hospitalization event during the study | 6 months (24 weeks) | No |
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