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Omega-3 Supplementation and Depression Clinical Trial

Role of Omega-3 Fish Oil Fatty Acids on Depression Among HIV-seropositive Pregnant Pregnant Women in Nairobi: A Randomized Double-blind Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01614249
Enrollment
216
Registered
2012-06-07
Start date
2012-06-30
Completion date
2014-01-31
Last updated
2018-06-28

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

Conditions

Depressive Symptoms

Keywords

Omega-3, EPA, Depression, HIV infected, Pregnant women

Brief summary

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.

Detailed description

Background to the study: Fatty acids are the key building blocks of most fats and oils, both those in the body and in foods. Among the essential fatty acids that are required to maintain health, but must come from the diet, is omega-3. These omega-3 fatty acids are important constituents of all cell membranes and are involved in the movement of substances in and out of the cells. They also produce hormone-like substances which regulate many functions of the body. The omega-3 fatty acids occur naturally, and consist of shorter long-chain alphalinolenic acid (ALA) and the longer chain, eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA). The ALA is naturally found in green leafy vegetables, flax seed, soybean oil and walnuts. The long chain EPA and DHA are naturally found in dark muscles of sea fish such as salmon, mackerel and tuna. These nutrients must be consumed in the diet because they cannot be synthesized by humans\[1\]. Research on the health benefits of omega-3 fatty acids dates back to 1929 when it was found to promote growth and prevent inflammation of the skin in rats \[2, 3\]. The essentiality of long-chain fatty acids for human health however emerged in 1970's when the first total parenteral nutrition which was fat-free was found to induce the essential fatty acid deficiencies among infants with volvulus, a bowel obstruction, at birth\[4\]. Further research in the 1970s on the health status of modern-hunter-gatherer Inuit Eskimos was also found to be related to their staple diet of fatty sea fish and fish eating marine mammals rich in long chain omega-3 fatty acids, EPA and DHA \[5\]. It has been proven that omega-3 long chain fatty acids, EPA and DHA improve depressive symptoms \[6, 7\]. As a mood disorder, depression is characterized by feelings of unhappiness and hopelessness, and generally marked by altered mood. It is not a single disease, but a syndrome encompassing a spectrum of symptoms with multiple causes \[8, 9\]. Women experience at least one episode of minor or major depression during pregnancy and after childbirth. This is however often under-diagnosed, undetected and missed out due to lack of screening. Although screening for depression may not be a routine activity in antenatal care, studies that have screened for depression in pregnancy indicate that 20-30% of pregnant women are depressed \[10, 11\]. The prevalence of depression is high during the second and third trimesters of pregnancy \[12\] when maternal level of omega-3 fatty acids is depleted. Adequate intake of long chain omega-3 fatty acids is also essential, during pregnancy to support normal growth and maturation of many fetal organ systems, particularly the brain and eyes \[13, 14\]. Moreover, long chain omega-3 fatty acids are critical for the development and function of many different organ systems of the fetus, including the structure of the brain and retina of the eye \[15\]. Premature birth and its potential neurological complications may result from omega-3 deficiency \[16\]. Documented research findings on omega-3 fatty acids and human immune-deficiency virus/ acquired immunodeficiency syndrome (HIV/AIDS) are mainly two-fold: one, on plasma triglycerides levels, and two, on the immune response parameters. Studies have shown that use of omega-3 fatty acids among HIV infected patients receiving highly active antiretroviral therapy is well tolerated and effective in reducing the plasma triglyceride levels \[17-19\]. The fish oil has therefore been recommended as second-line therapy for HIV patients with hypertriglyceridemia \[12\]. One of the metabolic end products of long chain fatty acids of omega-3 and omega-6, once eaten and absorbed by the body, are prostaglandin hormones which are responsible for the inflammation response. Research shows that omega-3 fatty acids produce less prostaglandin than omega-6 fatty acids, decreasing the inflammatory process \[5\]. Earlier research reported that omega-3 fish oil is immuno-suppressive as it significantly decreased various parameters of the immune response \[20\]. However, more recent studies have shown that dietary intake of omega-3 fatty acids increased the cluster of differentiation 4 (CD4) cell count \[21\] The role of long chain omega-3 fatty acids in combating depression among HIV-seropositive pregnant women has however not been established. The specific symptoms which may be more responsive to omega-3 supplementation have also not been established. 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 \[22\] and their health conditions as well as that of their unborn babies silently continue to deteriorate partly due to depression related comorbidities. This research will seek to ascertain that taking omega-3 fish oil supplement with higher EPA in relation to DHA can have a significant positive effect on depressive symptoms among HIV-seropositive pregnant women compared to a placebo. It will also monitor and identify those depressive symptoms that are more responsive to this nutrient among the HIV-seropositive pregnant women, and can be managed through nutrition supplementation. Conceptual Framework: The major risk factors for depression are genetic predisposition, hormonal imbalance and stressful events which could be of environmental, social or psychological origin as well as nutrition-related factors \[11, 23-25\]. Stressful events could however also cause hormonal imbalance, which, in the process can increase the stress hormone, cortisol, causing depression \[23\]. Both pregnancy and HIV infection status are also accompanied by high nutrient demand, in the presence of inadequate and inappropriate dietary intake as well as a high intake of saturated fats in fried food. This is likely to contribute to nutrient deficiencies, which also determines the neurotransmitter function and hormonal balance in mental health. Problem statement: This study seeks to ascertain that taking omega-3 fish oil supplement with higher EPA in relation to DHA have a significant positive effect on depressive symptoms among HIV-seropositive pregnant women. The level of omega-3 fatty acids rapidly declines during pregnancy as some of it is transferred to the fetus for the rapid formation of the fetal brain cells \[13\]. The resultant depletion in omega-3 might precipitate the occurrence of depression in pregnant women unless the nutrient deficit is met through dietary intake of omega-3 rich foods or supplementation. The modern diet is however inadequate in long chain omega-3 fatty acids \[5\]. About 40% of HIV-seropositive pregnant women are reportedly depressed \[26, 27\]. The depression in HIV-seropositive pregnant women is a significant public health problem due to its negative effects on both maternal and child health. It may adversely affect the quality of life and adherence to HIV/AIDS medication regimens \[27, 28\] which may subsequently affect disease progression and health outcome \[29\] of the women. Currently, more than 2 million pregnant women are estimated to be living with HIV infection globally \[9\]. In Kenya, about 9.0% of pregnant women are HIV-seropositive \[22\]. Justification of the study: This study will contribute to the debate on nutritional support and management of depressive symptoms and related health complications in HIV infected pregnant women and other vulnerable populations, to improve their mental health, hence improve the quality of life. A reduction in the prevalence of depression could therefore influence nutrition and health agencies as well as policy makers to make omega-3 fatty acid nutritional supplement accessible to HIV positive pregnant women and other vulnerable populations. Overall aim: To ascertain that taking omega-3 fish oil supplement with higher EPA in relation to DHA have a significant positive effect on depressive symptoms compared to a placebo among HIV-seropositive pregnant women. Research questions: 1.Does taking omega-3 fish oil supplement with higher EPA in relation to DHA have a significant positive effect on depressive symptoms among HIV-seropositive pregnant women, compared to a placebo? 2. Is the change in depressive symptom levels among study participants related to the change in their omega-3 fatty acid status after intervention with omega-3 fish oil supplement and placebo? 3. Which depressive symptoms are more responsive to omega-3 fish oil supplement intervention? Study setting: The study will be conducted at health facilities in Nairobi, Kenya. According to the latest Kenya national population and housing census results of 2009, \[30\], Nairobi, which is the capital city of Kenya, is the most populated city in the country with about 3.1 million people (about 1.6 million males and 1.5 million females) and an annual growth rate of about 4.1%\[16\]. The available sentinel survey data indicate that the prevalence of HIV/AIDS among pregnant women in Nairobi was 10.1% \[31\] in 2006. Methodology: This will be a double-blind, parallel randomized control trial (RCT) using omega-3 fish oil supplements and placebo. Both the study participants and the research administrators, including the principle investigator, will not know the difference between omega-3 supplement and placebo which will be of similar physical characteristics. Participants will be recruited from purposely sampled health facilities with highest attendance at the Prevention-of Mother-to-Child-Transmission (PMTCT) of HIV AIDS programs. The sampling frame will consist of pregnant women with known HIV-seropositive status and enrolled in PMTCT program at these health facilities. A total of 200 women who meet the study inclusion and exclusion criteria will be enrolled to participate in the study. Data Collection: Quantitative methods will be used to collect socio-demographic information, dietary intake data, and depressive symptoms, biological specimens of cheek cells, maternal weight, CD4 count, blood pressure and compliance with routine medication and study intervention. The primary measurement tool for efficacy of omega-3 fish oil will be the Beck Depression Inventory, Second Edition (BDI-II) scoring scale with a cut-off score for depression of 14 or more. Further understanding of depression in pregnancy and HIV/AIDS condition will be gained through qualitative methods. Cheek cell samples will be collected through mouth wash method for laboratory extraction of lipids for omega-3 analysis. The lipids will be extracted from the cheek cells using Bligh and Dyer methodology \[32\]. Gas-liquid chromatography by the method of Gibson and Kneebone \[33\] will be used to determine per cent (%) levels of omega-3 fatty acids in the lipids before, during and after the intervention.

Interventions

DIETARY_SUPPLEMENTSoybean oil soft gels

Each participant will receive OmegaVia soybean oil soft gels to take orally, one soft gel taken three times per day in the morning, mid-day and in the evening after meals for a period of 8 weeks

DIETARY_SUPPLEMENTFish oil omega-3 EPA-rich soft gels

A total of 3.0g of OmegaVia fish oil omega-3 EPA-rich soft gels will be taken orally per day as one soft gel in the morning, mid-day and evening after meals for 8 weeks with bi-weekly follow-up visits.

Sponsors

Consortium for Advanced Research Training in Africa (CARTA)
CollaboratorUNKNOWN
Innovix Pharma Inc.
CollaboratorUNKNOWN
University of Nairobi
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
15 Years to 49 Years
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Change in BDI-II Depressive Symptom Scores8 weeksDepressive 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.

Countries

Kenya

Participant flow

Recruitment details

Women who met the trial inclusion criteria were recruited from clinic registers at their respective Prevention of mother-to-child transmission program clinics from July 2012 to May 2013 with assistance from mentor-mothers in the clinics. Women visiting the clinics first time were included in clinic registers and invited to participate in the trial.

Pre-assignment details

Participants were assigned to either of the trial arms soon after enrollment to minimize drop-outs which might have occurred if enrolled participants exceeded gestation age or gave birth before randomization.

Participants by arm

ArmCount
Soybean Oil Soft Gels Control Group
As a control group, participants received OmegaVia soybean oil soft gels for eight weeks with regular cell-phone and bi-weekly face-to-face follow-up visits. During each follow-up visit, participants were re-supplied with soft-gels and monitored for side effects and compliance. Each participant randomly received a sequentially numbered, securely sealed opaque plastic bottle containing soybean oil soft gels to take for two weeks before returning for re-supply. Three soft gels of soybean oil were taken by each participant per day. Each soft gel contained saturated fatty acids (0.178 grams), monounsaturated fatty acids (0.299 grams) and polyunsaturated fatty acids (0.985 grams) with traces of eicosapentaenoic acid (EPA), of 0.115 grams. The soft gels were taken orally, one soft gel taken three times per day in the morning, mid-day and in the evening after meals for a period of 8 weeks.
107
Fish Oil Omega-3 EPA-rich Soft Gels Experimental Group
As the intervention group, participants received a dietary supplement of Omega Via fish oil omega-3 EPA-rich soft gels to take orally for eight weeks with bi-weekly follow-up visits to resupply the soft-gels, monitoring of side effects and compliance and data collection. Each participant randomly received a sequentially numbered, securely sealed opaque plastic bottle containing fish oil omega-3 EPA-rich soft gels to take for two weeks before returning for re-supply. Each participants took three soft gels of fish oil omega-3 fatty acid per day, each containing more EPA (0.715 grams) than docosahexaenoic acid (DHA) of 0.340 grams. The soft gels were taken orally, one soft gel taken three times per day in the morning, mid-day and in the evening after meals for a period of 8 weeks.
109
Total216

Withdrawals & dropouts

PeriodReasonFG000FG001
Overall StudyLost to Follow-up1123

Baseline characteristics

CharacteristicTotalSoybean Oil Soft Gels Control GroupFish Oil Omega-3 EPA-rich Soft Gels Experimental Group
Age, Categorical
<=18 years
10 Participants5 Participants5 Participants
Age, Categorical
>=65 years
0 Participants0 Participants0 Participants
Age, Categorical
Between 18 and 65 years
206 Participants102 Participants104 Participants
Age, Continuous26 Years26 Years26 Years
BDI-II depressive symptom scores21 Scores on a scale21 Scores on a scale20 Scores on a scale
Cluster of differentiation 4 (CD4) cell count360 cells/µl360 cells/µl361 cells/µl
Dietary calcium
At least EAR for pregnant women
59 participants28 participants31 participants
Dietary calcium
Below Estimated Average Requirement (EAR)
157 participants79 participants78 participants
Dietary folate
At least EAR for pregnant women
27 participants16 participants11 participants
Dietary folate
Below Estimated Average Requirement (EAR)
189 participants91 participants98 participants
Dietary Iron
At least EAR for pregnant women
0 participants0 participants0 participants
Dietary Iron
Below Estimated Average Requirement (EAR)
216 participants107 participants109 participants
Dietary selenium
At least EAR for pregnant women
58 participants31 participants27 participants
Dietary selenium
Below Estimated Average Requirement (EAR)
158 participants76 participants82 participants
Dietary total omega-3
At least recommended daily intake
28 participants18 participants10 participants
Dietary total omega-3
Below Recommended daily intake
188 participants89 participants99 participants
Dietary vitamin B1
At least EAR for pregnant women
76 participants40 participants36 participants
Dietary vitamin B1
Below Estimated Average Requirement (EAR)
140 participants67 participants73 participants
Dietary vitamin B12
At least EAR for pregnant women
25 participants13 participants12 participants
Dietary vitamin B12
Below Estimated Average Requirement (EAR)
191 participants94 participants97 participants
Dietary vitamin B6
At least EAR for pregnant women
44 participants20 participants24 participants
Dietary vitamin B6
Below Estimated Average Requirement (EAR)
172 participants87 participants85 participants
Dietary vitamin C
At least EAR for pregnant women
95 participants48 participants47 participants
Dietary vitamin C
Below Estimated Average Requirement (EAR)
121 participants59 participants62 participants
Dietary vitamin E
At least EAR for pregnant women
40 participants20 participants20 participants
Dietary vitamin E
Below Estimated Average Requirement (EAR)
176 participants87 participants89 participants
Dietary zinc
At least EAR for pregnant women
2 participants2 participants0 participants
Dietary zinc
Below Estimated Average Requirement (EAR)
214 participants105 participants109 participants
Education status
At least High school education
106 participants52 participants54 participants
Education status
No High school education
110 participants55 participants55 participants
Employment status
In gainful employment with income
91 participants43 participants48 participants
Employment status
Not in gainful employment
125 participants64 participants61 participants
Experienced stressful life event
None 2 weeks before study
148 participants75 participants73 participants
Experienced stressful life event
Yes, 2 weeks before study
68 participants32 participants36 participants
Gestation age22 Weeks22 Weeks22 Weeks
HIV status disclosure to anyone
Disclosed to someone
173 participants82 participants91 participants
HIV status disclosure to anyone
Not disclosed
43 participants25 participants18 participants
HIV status knowledge before pregnancy
No, newly tested less than 6 months
112 participants56 participants56 participants
HIV status knowledge before pregnancy
Yes, known positive, 6 months plus
104 participants51 participants53 participants
Household income per month5050 Kenya Shillings (Ksh.)5025 Kenya Shillings (Ksh.)6000 Kenya Shillings (Ksh.)
Marital status
Married
167 participants85 participants82 participants
Marital status
Single (not married, divorced, widowed
49 participants22 participants27 participants
Mid-upper-arm circumference (MUAC)26.0 cm26.0 cm26.0 cm
Parity
First pregnancy
48 participants24 participants24 participants
Parity
Not first pregnancy
168 participants83 participants85 participants
prevention of mother-to-child transmission program m2m support group meeting attendance
Attended
100 participants53 participants47 participants
prevention of mother-to-child transmission program m2m support group meeting attendance
Not attended
116 participants54 participants62 participants
Region of Enrollment
Kenya
216 participants107 participants109 participants
Sex: Female, Male
Female
216 Participants107 Participants109 Participants
Sex: Female, Male
Male
0 Participants0 Participants0 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
— / —— / —
other
Total, other adverse events
15 / 10724 / 109
serious
Total, serious adverse events
0 / 1070 / 109

Outcome results

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.

Time frame: 8 weeks

Population: Only participants who completed the 8-weeks trial period were included in the final analysis of primary outcome. Per protocol analysis Post-intervention BDI-II scores at week 8 minus baseline BDI-II scores at week 0

ArmMeasureValue (MEAN)
Soybean Oil Soft Gels Control GroupChange in BDI-II Depressive Symptom Scores-13.9 scores on BDI-II scale
Fish Oil Omega-3 EPA-rich Soft Gels Experimental GroupChange in BDI-II Depressive Symptom Scores-13.3 scores on BDI-II scale
Comparison: Null hypothesis: There is no difference in the magnitude of change in BDI-II scores between HIV-seropositive pregnant women on fish oil omega-3 EPA-rich supplements and the control group on soybean oil soft gels. A sample size of 91 women per arm gave an 85% power to detect as statistically significant at 5% level, a true difference of 4 scores in the mean depressive symptom scores between the two arms assuming a within group standard deviation of nine in depressive symptom scores.p-value: 0.2195% CI: [-0.58, 2.6]ANCOVA

Source: ClinicalTrials.gov · Data processed: Feb 23, 2026