Agra

This research aims to evaluate the use and safety of Motiva Implants in people undergoing breast implant procedures. The study focuses on collecting and assessing safety and effectiveness data about these implants after they have been approved and are in general use. It includes participants who have primary breast augmentation, revision breast augmentation, or other aesthetic surgeries, with a focus on female patients aged 22 and older. Participants will receive Motiva Implants as part of their breast surgery or undergo other aesthetic procedures. The study is prospective and non-randomized, with data collected at baseline before surgery, during the operation, and annually for up to 10 years after surgery. Participants who have revision surgery or other aesthetic procedures without implants are also included as control groups to compare outcomes. During the study, participants will have various assessments including medical imaging such as CT, ultrasound, or MRI if medically advised. Researchers will monitor for connective tissue disease signs and symptoms, reproductive complications, cancer diagnoses, local complications, and patient satisfaction over 10 years. The impact of RFID on imaging will also be assessed. Participants will be followed for up to 10 years, providing long-term data on the safety and performance of Motiva Implants.

Researchers are evaluating a prescribed sub-symptomatic adaptable exercise treatment SAET for active duty service members with persistent cognitive complaints following mild traumatic brain injury mTBI. The study aims to see if SAET can reduce symptoms, improve mental health, enhance physiological functioning, and help participants return to duty. It compares SAET to a control group doing stretching exercises to determine which approach better reduces neurobehavioral symptoms and improves cognitive and physical performance. Participants will be randomly assigned to either the SAET group or the stretching control group SCG. Both groups will attend two in-clinic sessions per week with a licensed Physical Therapist or Exercise Physiologist and complete three independent sessions weekly for eight weeks, totaling 40 hours. SAET sessions include stretching, aerobic exercise, resistance training, and mobility work, adjusted to keep symptoms below noticeable levels. Stretching sessions focus on static stretches and yoga-based movements without raising heart rate. During the study, participants will undergo assessments of neurobehavioral symptoms, cognitive function, physiological adaptation, and military performance at baseline, post-treatment, and three months after treatment ends. Researchers will monitor heart rate variability, oxygen consumption, cerebrovascular blood flow, and physical fitness using tests such as the Marine Corps Combat Fitness Test. Participants will also complete questionnaires about their exercise habits. The study lasts about six months and includes safety monitoring and follow-up assessments to measure treatment effects over time.