Obesity is associated with chronic inflammation, which increases the risk for other metabolic diseases. Omega-3 fatty acids and their derivatives have anti-inflammatory properties but are reduced in people who are overweight or obese. The purpose of this study is to determine if omega-3 fatty acid supplementation (SPM Active) for 3 months can effectively increase the biological levels of its lipid components in adult males who are overweight or obese. Additionally, we will determine if supplementation with SPM Active can improve mental health outcomes, as measured by validated surveys.

This study compares a video-watching treatment for amblyopia to patching only, for children ages 4-7 years with this diagnosis.

To better understand the factors that affect consumers' purchasing decisions in a convenience store environment.

This study is being conducted to evaluate the current state of knowledge regarding long-term child outcomes among children born to women with mild CHTN who received antihypertensive therapy in pregnancy or who had preeclampsia. This study will compare long-term outcomes, including neurodevelopment and growth in women who participated in the CHAP study with pregnancy.

Investigate the safe wearability and basic functions of the multi-modality sensors fabricated in the PI lab.

The purpose of this study is to understand more about the evolving practices of evangelical contemporary worship and perceptions of such practices by church leaders versus worship participants.

We are hoping to have patient who under went doulbe-jaw surgery for obstructive sleep apnea fill out a survey to inform of us there experience, expectations, and results after surgery.

This clinical trial aims to understand how well ALXN-C5IT works over a long time. We want to see if it can prevent relapses and help with disability, walking, and vision. We also want to know how patients feel about their health while using ALXN-C5IT.

Purpose: This exploratory study aims to examine characteristics and patterns of victimization experiences and protective factors during youth through the life history calendar (LHC) method with a sample of young adults. Participants: This study will recruit 25 young adults (ages 18-24) who are of a racial or ethnic minoritized identity. Potential participants must also endorse experiencing at least two victimizations prior to the age of 18 that occurred over two months in duration and at least one victimization experience rated as having had a moderately severe impact on the individual. Procedures: Participants will retrospectively reflect on their victimization experiences (onset, duration, perceived severity of impact) and perceived protective factors during childhood and early adolescence (< 18 years old) through the completion of an LHC interview.

The purpose of this study is to validate a new voice-enabled tablet to ensure it is an accurate and acceptable way to administer PROs questionnaires in Malawi. This voice-enabled tablet was developed specifically for patient populations who are unable to comfortably read and write, so that they can have equal access to participating in direct self-reporting their own PROs Questionaries without needing and interviewer to assist them. Once validated in the first 50 participants, then we will continue to enroll 500 participants who will take the PROMIS-25 and/or PRO-CTCAE Questionnaires at various time points throughout their treatment. This will allow you to directly self-complete the PRO surveys and give you a voice so that your struggles, quality of life, and symptoms can be more accurately and comprehensively communicated to the medical care team. We hope that through administering these PROs questionnaires, it will also improve the overall care, management of