Fort Worth, TXNCT07688720Now EnrollingIRB Ready

Perimenopause Clinical Trial in Fort Worth, TX

Access cutting-edge perimenopause treatment through this clinical trial at a research site in Fort Worth. Study-provided care at no cost to qualified participants.

Sponsored by Texas Christian University

Quick Self-Assessment

See if you qualify for this Fort Worth location

Preparing your pre-screening questions…

Expert Care in Fort Worth

Access perimenopause specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related perimenopause treatment provided free

Apply for This Fort Worth Location

Check if you qualify for this perimenopause clinical trial in Fort Worth, TX

Secure & Confidential

Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Fort Worth

    Convenient for TX residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Fort Worth site if eligible
  4. 4Begin participation

About This Perimenopause Study in Fort Worth

Transcutaneous Auricular Neurostimulation (tAN) will be administered to women with premenstrual syndrome (PMS), premenstrual dysphoric disorder (PMDD), and perimenopause. The investigators will examine whether tAN improves symptomology by collecting self-report data before the intervention, during the intervention, and following the intervention.

Sponsor: Texas Christian University

Who Can Participate

Inclusion Criteria

Assigned female at birth
Age 18 to 45
Naturally cycling
Regularly occurring menstrual cycle
Must identify as having PMS or PMDD
Reliable ability to complete online study surveys

Exclusion Criteria

Using hormonal birth control
Pregnant or lactating/breastfeeding
History of seizures
Implanted devices
Current or previous diagnosis of any heart conditions
Abnormal ear anatomy
Non-removable piercings on the ear
Recent ear infection
Taking SSRIs
Taking steroids
Taking hormone therapy
If the participant anticipates starting or stopping prescription medications during the study period
Participant has a history of neurologic diseases (i.e. stroke, brain tumor, cerebrovascular, etc.)
Participant has a history traumatic brain injury within the past 12 months
Must not have any other mental illness or mood disorder Perimenopause Study: Inclusion Criteria:
Assigned female at birth.
Age 40 to 55
Must have newly variable menstrual cycles or report identifying as perimenopausal
Reliable ability to complete online study surveys Exclusion Criteria:
Using hormonal birth control
Pregnant or lactating/breastfeeding
History of seizures
Implanted devices
Current or previous diagnosis of any heart conditions
Abnormal ear anatomy
Non-removable piercings on the ear
Recent ear infection
Taking SSRIs
Taking steroids
Taking hormone therapy
If the participant anticipates starting or stopping prescription medications during the study period.
Participant has a history of neurologic diseases (i.e. stroke, brain tumor, cerebrovascular, etc.)
Participant has a history traumatic brain injury within the past 12 months
have a hysterectomy In both studies we will confirm that participants are symptomatic shortly following enrollment.

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Fort Worth?

Yes, this clinical trial (NCT07688720) has an active research site in Fort Worth, TX that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Perimenopause Treatment Options in Fort Worth, TX

If you're searching for perimenopause treatment options in Fort Worth, TX, this clinical trial (NCT07688720) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Fort Worth research site is actively enrolling participants for this clinical trial. You'll receive care from experienced perimenopause specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all perimenopause clinical trials near you to find additional studies recruiting in your area.

More Pulmonary Embolism Trials in Fort Worth, TX

See all pulmonary embolism clinical trials recruiting in Fort Worth — not just this study.

Browse Pulmonary Embolism Trials in Fort Worth →

Browse More Trials by Condition

Pulmonary Embolism TrialsMenopause TrialsMyalgic Encephalomyelitis TrialsAll Conditions →

Ready to Join in Fort Worth?

Take the first step toward participating in this groundbreaking clinical trial

Secure · Expert Care · Fort Worth, TX