Depressive Symptoms Clinical Trial
Official title:
Role of Omega-3 Fish Oil Fatty Acids on Depression Among HIV-seropositive Pregnant Pregnant Women in Nairobi: A Randomized Double-blind Controlled Trial
Verified date | May 2018 |
Source | University of Nairobi |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Fish oil omega-3 supplements provide essential nutrients for brain health and functioning.
These nutrients have been proven to be effective in reducing depressive symptoms. They have
also been found to be effective and well tolerated in reducing the bad fat accumulation among
patients infected with human immunodeficiency virus (HIV)and are using highly active
antiretroviral treatment. The role of this nutritional supplement in combating depression
among pregnant women who are living with HIV infection has however not been established. Yet,
currently, more than 2 million pregnant women are estimated to be living with HIV infection
globally. In Kenya, about 9.0% of pregnant women are HIV-seropositive.
In this study, it is hypothesized that there is no difference in the levels of depressive
symptoms among HIV infected pregnant women who are taking omega-3 fish oil supplements and
those taking a placebo.
The study will therefore seek to ascertain that taking omega-3 fish oil nutritional
supplement has a significant positive effect on depressive symptoms among HIV infected
pregnant women, compared to a placebo.
Status | Completed |
Enrollment | 216 |
Est. completion date | January 2014 |
Est. primary completion date | July 2013 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 15 Years to 49 Years |
Eligibility |
Inclusion Criteria: - All pregnant HIV seropositive women with known CD4 cell count less than 500 - Pregnant women who are in their 2nd trimester of pregnancy (Week 13-27). - Normal nutritional status pregnancy with mid-upper arm circumference (MUAC of 22 cm - 33 cm)at entry into the study; - Beck Depression Inventory Second Edition (BDI-II) Scale scores at entry into the study of 14 or more; - Pregnant HIV positive women who will give consent to participate in the study Exclusion Criteria: - Underweight with MUAC less than 22 cm and overweight with MUAC more than 33 cm at entry into the study; - Pregnant women taking antidepressant medications; - Those on anti-clotting medication (those with liver disease, varicose veins, peptic ulcers); or Vitamin K supplement. Omega-3 supplements may increase their effects; - Those on diabetic medication since Omega-3 may increase their blood sugar. - Incomplete depression screening form (more than 5 items unanswered) - Those whose BDI-II screening scores are less than 14; - Those women currently taking omega-3 nutritional supplement - Pregnant HIV-seropositive women without consent to participate in the study. |
Country | Name | City | State |
---|---|---|---|
Kenya | Nairobi City Council Health Facilities | Nairobi |
Lead Sponsor | Collaborator |
---|---|
University of Nairobi | Consortium for Advanced Research Training in Africa (CARTA), Innovix Pharma Inc. |
Kenya,
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* Note: There are 33 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in BDI-II Depressive Symptom Scores | Depressive symptoms were assessed by Beck Depression Inventory Second Edition (BDI-II) Scoring scale at Baseline and end of study during the 8- week study period. The BDI-II Scale is a 21-item scoring tool which measures the existence and severity of symptoms of depression. Each of the 21 items on BDI-II tool represent a depressive symptom. The symptoms are each scored on a 4-point Likert scale of 0 to 3 (0=symptom is absent; 3=symptom is severe).Scores for each symptom are added up to obtain the total scores for all 21 items, which are interpreted as follows: Scores of 0-13: minimal depression; 14-19: mild depression; 20-28: moderate depression and 29-63: severe depression. The change in BDI-II scores were computed from post-intervention scores at week 8 and baseline BDI-II scores at week 0. | 8 weeks |
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