Hormones, Outcomes, and Pain Pathways in Exercise Study
University of Houston · with National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), The University of Texas Health Science Center, Houston · NCT07579182
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18–60 · Women only
- Healthy volunteers
- Accepted
- Study type
- Interventional · Phase 1
- Target enrollment
- 140
- US sites recruiting
- 1
- Study start
- May 17, 2026
- Record last updated
- June 2, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
The goal of the proposed project is to evaluate a mechanical intervention (sports bras designed specifically for full busted women) to alleviate neck, shoulder, arm, and back pain in full-busted women and investigate the contribution of non-mechanical pathways associated with this type of pain in women. Specifically, the investigators will investigate how sex-hormones, inflammation, and remapping of specific regions of the brain contribute to the manifestation of neck, shoulder, arm, and back pain in full-busted women across the lifespan.
Being studied: Interventional Sports bra
Conditions: Breast Pain; Mastalgia; Back Pain; Back Pain, Low; Neck Pain; Chest Pain; Activity, Motor; Healthy Aging; Weight, Body; Inflammation; Gonadal Steroid Hormones; Neuronal Plasticity; Neuromuscular Manifestations
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Able to provide informed consent
- Age of 18 to 60 years
- Assigned female sex at birth
- Right-handed by self-declaration
- Willing to participate in one online testing session and up to four in-person testing sessions
- Bra band size between 32-40"
- International Physical Activity Questionnaire - Short Form (IPAQ-SF) score of 2 or higher
- An answer of "NO" to any item of the general health questions of the PARQ+
- No history of surgery to the: back, neck, or shoulders or joint replacement
- No history of implanted pacemakers or other stimulation devices
- No history of spinal cord injury (SCI)
Exclusion Criteria
- Inability to provide informed consent
- Age 17 years old or younger or 61 years or older
- Assigned male sex at birth
- Left-handed by self-declaration
- Not willing to participate in one online testing session and up to four in-person testing sessions
- Bra band size greater than 40" or less than 32"
- IPAQ-SF score of 1 or lower
- An answer of "YES" to any item of the general health questions of the PARQ+
- History of limb amputation (upper or lower extremity)
- Presence of open pressure sores on the upper or lower extremities
- Currently pregnant or lactating/breastfeeding
- History of surgery to the: back, neck, or shoulders or joint replacement
- History of breast cancer and/or mastectomy
- History of implanted pacemakers or other stimulation devices
- History of spinal cord injury (SCI)
- History of joint disease including osteoarthritis and/or Rheumatoid Arthritis
- History of the following neurological diseases: Cerebrovascular accident (CVA, stroke), Alzheimer's Disease (AD), Dementia (of any form), Huntington's Disease, Traumatic Brain Injury (TBI), Spinal cord injury (SCI), Multiple Sclerosis (MS), Parkinson's Disease (PD), Polio, Paraproteinaemic Demyelinating Neuropathy (PDN) and/or Monoclonal Gammopathy of Undetermined Significance (MGUS), Myasthenia Gravis, Muscular Dystrophy, Guillain-Barré Syndrome, Scoliosis, Charcot-Marie-Tooth Disorder or other hereditary neuropathies
Additional Inclusion Criteria for Intervention Group:
a. Self-declared breast size of D-I cup (US sizes: D, E, F, G, H)
Additional Inclusion Criteria for the Control Group:
a. Self-declared breast size of A-C cup (US sizes: AA, A, B, C)
Recruiting US locations
University of Houston
Houston, TX 77204
Site contact: Stacey L Gorniak, PhD · 713-743-4802 · sgorniak@uh.edu
Study contacts (from the official record)
- Stacey L Gorniak, PhD · 713-743-4802 · sgorniak@uh.edu
Similar studies in Texas
All weight loss studies in Texas →- RecruitingHealthy volunteersPhase 1Overnight stay mentioned
A Study of Eloralintide (LY3841136) in Participants With Obesity or Overweight
Eli Lilly and Company
- Location
- San Antonio, TX
- Eligibility basics
- Ages 18–65
- RecruitingHealthy volunteersPhase 1
A Study of LY4174794 in Participants With Obesity or Overweight Who Are Otherwise Healthy
Eli Lilly and Company
- Location
- San Antonio, TX
- Eligibility basics
- Ages 18–65
- RecruitingHealthy volunteersPhase 1
A Study of Eloralintide (LY3841136) in Female Participants With Obesity or Overweight
Eli Lilly and Company
- Location
- Dallas, TX + 1 other US site
- Eligibility basics
- Ages 18–60 · Women only
- RecruitingHealthy volunteersPhase 1
A Study of LY4329090 in Participants With Obesity or Overweight Who Are Otherwise Healthy
Eli Lilly and Company
- Location
- Dallas, TX + 1 other US site
- Eligibility basics
- Ages 18–65