University of North Carolina at Chapel Hill
Chapel Hill, North Carolina, 27599, United States
NCT Number: NCT06899074
The purpose of the study is to assess the biochemical and clinical effects of omega-3 polyunsaturated fatty acid (PUFA) supplementation in youth suffering from migraine, including its effects on migraine disability, psychological distress, and overall quality of life. This study duration 12 weeks.
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Notify Me10 year–17 year
All sexes
Interventional
Not applicable
Chapel Hill, North Carolina, 27599, United States
Omega-3 polyunsaturated fatty acids (PUFAs), particularly eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), hold potential therapeutic benefit for pediatric migraine due to their potent anti-inflammatory, anti-nociceptive, and neuromodulatory properties, which impact the pathophysiology of migraine. Dietary alteration and supplementation of omega-3 PUFAs have been shown to decrease the frequency, duration, and severity of headaches in adults with migraine, yet no rigorous clinical studies on omega-3 polyunsaturated fatty acid (PUFA) supplementation have been conducted in children and/or adolescents suffering from migraine. This study will establish feasibility of the intervention of omega-3 PUFA supplementation for pediatric migraine (i.e., provide proof-of-concept that the intervention raises omega-3 index levels compared to placebo).
The investigators will enroll children and adolescents (ages 10-17 years) with a diagnosis of migraine and randomize participants 1:1 to receive an omega-3 PUFA dietary supplement intervention or placebo daily for 12 weeks, with assessments conducted at baseline and at 12 weeks.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Omega-3 PUFA dietary supplement daily for 12 weeks. The intervention is 1 teaspoon of liquid omega-3 containing oil profile 40% EPA / 60% DHA.
The placebo is a matched 1 teaspoon liquid of coconut oil, consisting mainly of saturated fatty acids and lacking omega-3 fatty acids.
Other names: Coconut oil
Time frame: Baseline and 12 weeks
The Omega-3 Index is defined as the combined percentage of eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) in red blood cell membranes, expressed as a percentage of total fatty acids. Possible range: 0-100%. Higher values indicate greater incorporation of omega-3-fatty acids (favorable outcome). This outcome compares the change in omega-3 index levels via finger prick blood test.
Time frame: Baseline and 12 weeks
The associations between omega-3 (O3) index levels and pain intensity will be assessed based on validated self-report measures using the Patient-Reported Outcomes Measurement Information System (PROMIS) Pediatric Pain Intensity Measure (PPIM). The PROMIS Pain Intensity instruments assess how much the child hurts. The PROMIS Pediatric Pain Intensity Measure is a 3-item, self-report measure for children and adolescents ages 8 to 18 with chronic pain, using a 5-point Likert scale including three items rating pain from "Had no pain" = 1 to "Very severe" = 5. Total raw scores for the short form are summed for the values of the response to each question. Raw score range: 3-15. Raw scores are then converted to t-scores using a standardized scale where 50 represents the average of the general US population, and each 10-point difference represents one standard deviation. T-score range: 26.8-74.1. Higher scores indicate worse or more intense pain.
Time frame: Baseline and 12 weeks
The associations between omega-3 index levels and pain interference will be assessed based on validated self-report measures using the Patient-Reported Outcomes Measurement Information System (PROMIS) Pediatric Pain Interference Scale (PPIS). The PROMIS Pediatric Pain Interference Scale is an 8-item self-report questionnaire completed by children that assesses how pain impacts a child's daily activities of living and the enjoyment of those activities using a 5-point likert scale. This survey is measured on a scale of 1-5, from 1 being never to 5 being almost always. A lower score will indicate less pain interference in the pediatric patient. Raw scores are then converted to t-scores using a standardized scale where 50 represents the average of the general US population, and each 10-point difference represents one standard deviation. T-score range: 43.8-83.5.
Time frame: Baseline and 12 weeks
The validated Pediatric Migraine Disability Assessment tool (PedMIDAS) was used to measure migraine disability by self-report. PedMIDAS was developed to assess migraine disability in pediatric and adolescent patients ages 4-18. It is intended to be self-administered by the patient and their parent. The PedMIDAS is scored by summing the answers across 6 questions. The raw score ranges from 0 (minimum) to 240 (maximum). Higher scores reflect greater headache-related disability, with clinical cut-off scores graded 0-10 indicating "little to none", 11-30 indicating "mild", 31-50 indicating "moderate", or greater than 50 indicating "severe" migraine disability. The number of participants meeting each category was recorded.
Time frame: Baseline and 12 weeks
The validated Revised Children's Anxiety and Depression Scale (RCADS)-short version will be used to measure psychological distress by self-report. The RCADS is a 25-item questionnaire designed to assess symptoms of anxiety and depression in children and adolescents aged 8 to 18 years using a 4-point Likert scale. Each item is assigned a numerical value from 0-3, where 0 = Never, 1 = Sometimes, 2 = Often, and 3 = Always, with a raw score range of 0 to 75. Raw scores are converted to standardized T-scores based on their age (grade level) and gender. T-score range: 24-163. RCADS T-scores a reported with a standardized mean of 50 and a standard deviation of 10. A higher T-score indicates a higher level of anxiety and/or depression in the pediatric patient. These standardized scores indicate the severity of their symptoms compared to peers in the general population. T-scores < 65 indicate normal or low severity; T-scores of 65-69 are borderline; T-scores >/= 70 are clinical severity.
University of North Carolina, Chapel Hill
Other
Evaluating the Effects of Omega-3 Polyunsaturated Fatty Acids in Pediatric Migraine Patients
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