Whittier, CANCT07285707Now EnrollingIRB Ready

Long COVID Clinical Trial in Whittier, CA

Access cutting-edge long covid treatment through this clinical trial at a research site in Whittier. Study-provided care at no cost to qualified participants.

Sponsored by Southern California University of Health Sciences

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Expert Care in Whittier

Access long covid specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related long covid treatment provided free

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Check if you qualify for this long covid clinical trial in Whittier, CA

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Why Participate?

  • No-Cost Study Care

  • Local to Whittier

    Convenient for CA 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 Whittier site if eligible
  4. 4Begin participation

About This Long COVID Study in Whittier

List of the Hypothesis: Primary hypothesis: A flexible acupuncture and Chinese herbal medicine protocol will be feasible, acceptable, and useful for the treatment of long COVID. Secondary hypothesis: Long COVID patients receiving acupuncture treatment or acupuncture treatment and Chinese herbal supplements over an 8-week period will see improvements in their symptoms, function, and quality of life measurements. Specific Aims of This Research (Purpose of the study): To study the feasibility, acceptability and utility of an acupuncture and Chinese herbal supplement treatment protocol for patients with long COVID and preliminarily assess the effects of treatment. Currently Available Research on This Subject: Studies indicate that acupuncture can effectively treat symptoms that are similar to those often seen in long COVID patients. Additionally, recent studies and clinical evidence suggest that there is substantial potential for acupuncture in the treatment of long COVID. Acupuncture may be beneficial because it can address many symptoms simultaneously with a single intervention, whereas symptom clusters can be difficult to manage with pharmaceuticals due to the need for multiple pharmaceutical agents. Summary of the research protocol/methodology: Five patients will receive acupuncture treatment, and five patients will receive acupuncture and Chinese herbal medicine. Each participant will receive 16 acupuncture treatments over the course of eight weeks (i.e., twice per week). Each treatment session will last for 30 minutes. Follow-up will occur at 12 weeks (i.e., four weeks after the final treatment session). Significance of this research to the health and welfare of general public: There is currently not a single, specific treatment for long COVID. If acupuncture treatment alone and/or acupuncture and Chinese herbal medicine combined are feasible, acceptable, and efficacious in the improvement of long COVID symptoms, it will offer patients additional treatment options, which may help some patients to avoid pharmaceutical treatment side effects or polypharmacy challenges.

Sponsor: Southern California University of Health Sciences

Who Can Participate

Inclusion Criteria

18 years of age or older
We will include adults of any age in our study. Adults of all ages can experience long COVID symptoms, although it is more common in older adults • Confirmed and documented COVID-19 illness (confirmed by healthcare provider or test; acceptable documentation includes but is not limited to a doctor's note or a photo of test result)
COVID-19 illness is a necessary precursor to the development of long COVID • Experiencing at least one of the following common long COVID symptoms for at least 4 weeks after confirmed COVID-19 illness:
Fatigue or post-exertional malaise,
Dyspnea, cough,
Brain fog, sleep disturbance, depression, anxiety,
Arthralgia, myalgia, or
Constipation, diarrhea, stomach pain
Over 200 different long COVID symptoms have been identified. The proposed study is a small pragmatic pilot study which only plans to enroll 10 participants. It is necessary to limit inclusion to some of the most common symptoms to ensure that the findings are broadly relevant across the long COVID patient population.
The symptoms were not present prior to the confirmed COVID-19 illness o If the symptoms were present prior to the confirmed COVID-19 illness, then they are most likely attributable to a cause other than long COVID
Willingness to comply with the treatment schedule o It is important that all those who qualify for the study are willing to comply with the protocol that is being adopted. If the patient is not willing to attend acupuncture treatment sessions or comply with the supplement schedule, then they may not be enrolled in the study.
Ability to read and understand English o Informed consent will be in the English language. Inability to read and understand English will interfere with provision of informed consent. Moreover, compliance is a potential issue with herbal supplementation. Recruiting patients who are able to read and understand English instructions for supplement intake will help to improve compliance with the protocol.
Ability to provide informed consent o It is important that participants are aware that they are required to provide written informed consent before they are allowed to participate. Some individuals who are eligible might be unwilling to sign the informed consent form.

Exclusion Criteria

• Under 18 years of age
Pulmonary fibrosis or on continuous oxygen treatment
Certain preexisting conditions:
Diagnosed with Alzheimer's or demonstrating onset of dementia
Uncontrolled hypertension, diabetes, or autoimmune conditions
Other comorbid conditions that might imitate long COVID symptoms
Undergoing cancer treatments
Use of acupuncture or Chinese medicine in the past three months
Involved in health-related litigation or legal claims
Missing either baseline visit and deemed unlikely to comply with the study protocol
Pregnant or breastfeeding or trying to get pregnant

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 Whittier?

Yes, this clinical trial (NCT07285707) has an active research site in Whittier, CA 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.

Long COVID Treatment Options in Whittier, CA

If you're searching for long covid treatment options in Whittier, CA, this clinical trial (NCT07285707) 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 Whittier research site is actively enrolling participants for this clinical trial. You'll receive care from experienced long covid 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 long covid clinical trials near you to find additional studies recruiting in your area.

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