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Recruiting EARLY_Phase 1 NCT06779188

NCT06779188 Examining the Effects of Theta Burst TMS on Brain Connectivity and Balance Ability in Older Adults With Balance Problems

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Clinical Trial Summary
NCT ID NCT06779188
Status Recruiting
Phase EARLY_Phase 1
Sponsor Weinberg Medical Physics LLC
Condition Aging
Study Type INTERVENTIONAL
Enrollment 30 participants
Start Date 2025-05-06
Primary Completion 2027-05-01

Eligibility & Interventions

Sex All sexes
Min Age 65 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Transcranial Magnetic StimulationTranscranial Magnetic Stimulation Sham

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

Phase 1 is the earliest stage of human testing — safety and dosage are the primary focus. Visits are frequent and medical supervision is intensive. You will be among the first people to receive this treatment.

This trial targets 30 participants in total. It began in 2025-05-06 with a primary completion date of 2027-05-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The goal of this study is to learn if manipulating the brain using magnets works to treat balance impairment, a major cause of falls, in older adults with balance problems. The technique to manipulate the brain using magnets is known as transcranial magnetic stimulation or TMS. The main questions this study aims to answer are: * How does TMS change communication between brain areas? * Does TMS improve balance ability in older adults with balance problems? Researchers will compare the TMS group to a placebo group to see if manipulating the brain using magnets works to treat balance impairment. Participants will: * Receive TMS or placebo stimulation for 4 weeks. * Visit the laboratory for checkups and tests 3 times.

Eligibility Criteria

Inclusion Criteria: a) Able to provide informed consent b) All ethnic groups c) \>65 years of age d) ≥2 non-injury falls or ≥1 injury fall in the past year \[17\]-\[21\] e) Absence of dementia/uncontrolled psychiatric disorder h) Able to walk and stand for 5 min continuously independently without assistance (i.e., cane, walker, ankle foot orthotics, electric scooter). i) Willingness to undergo MRI, participate in the 4-weeks intervention AND in the laboratory studies before, immediately-after, and 3-month after the intervention. Exclusion Criteria: 1. Inability to provide informed consent. 2. Non-English speaking. 3. Have contraindications to TMS based on TMS Adult Safety Screen (e.g., pregnancy, metal in the brain/skull, neurostimulator, pacemaker, infusion device, medication to treat mental illness) 4. Unintentional weight loss of ≥10 pounds over the past year. 5. Severe uncontrolled hypertension, or uncontrolled diabetes. 6. Poor cognitive status (Montreal Cognitive Assessment (MoCA) score ≥ 26) 7. Untreated depression or Geriatric Depression Scale score on 15 item scale \>7 8. History of limb amputation (upper or lower extremity) 9. Planned surgery in the next 3 months. 10. History of chemotherapy or planned chemotherapy in the next 6 months or active malignancy. 11. Severe osteoporosis, defined by diagnosis of osteoporosis with fracture. 12. Pregnant or have a chance of being pregnant. 13. Chronic inflammatory condition, autoimmune disease or infectious processes such as active tuberculosis, Human Immunodeficiency Virus, Rheumatoid arthritis, systemic lupus erythematosus, acute or chronic hepatitis B or C. 14. Illicit drug use 15. Use of medications that may increase the risk of falling: * Sedatives * Hypnotics * Anti-cholinergic * Benzodiazepines * Anti-depressants 16. Intracranial bleeds visible on their most recent CT or MRI scans.

Contact & Investigator

Central Contact

Pranav J Parikh, MBBS, PhD

✉ pjparikh2@uh.edu

📞 713-743-0503

Frequently Asked Questions

Who can join the NCT06779188 clinical trial?

This trial is open to participants of all sexes, aged 65 Years or older, studying Aging. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

What phase is the NCT06779188 trial and what does that mean for participants?

Phase 1 trials are the first stage of human testing. The primary goal is to assess safety and determine appropriate dosage levels. Participants are closely monitored. These trials typically involve a small number of volunteers.

Is NCT06779188 currently recruiting?

Yes, NCT06779188 is actively recruiting participants. Contact the research team at pjparikh2@uh.edu for enrollment information.

Where is the NCT06779188 trial being conducted?

This trial is being conducted at Houston, United States.

Who is sponsoring the NCT06779188 clinical trial?

NCT06779188 is sponsored by Weinberg Medical Physics LLC. The trial plans to enroll 30 participants.

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