Birmingham, ALNCT07149870Now EnrollingIRB Ready

Chronic Pain Clinical Trial in Birmingham, AL

Access cutting-edge chronic pain treatment through this clinical trial at a research site in Birmingham. Study-provided care at no cost to qualified participants.

Sponsored by VA Office of Research and Development

Quick Self-Assessment

See if you qualify for this Birmingham location

Preparing your pre-screening questions…

Expert Care in Birmingham

Access chronic pain specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related chronic pain treatment provided free

Apply for This Birmingham Location

Check if you qualify for this chronic pain clinical trial in Birmingham, AL

Secure & Confidential

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

Why Participate?

  • No-Cost Study Care

  • Local to Birmingham

    Convenient for AL 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 Birmingham site if eligible
  4. 4Begin participation

About This Chronic Pain Study in Birmingham

The focus of this study is to determine whether adding Whole Health Coaching (WHC) improves pain care among adults with chronic pain and who are currently working with a pain management team (PMT) at the VA.

Sponsor: VA Office of Research and Development

Who Can Participate

Inclusion Criteria

High-impact chronic pain (defined using the Graded Chronic Pain Scale - Revised). -AND-
Active prescription for LTOT (\>90 days continuous prescription). -AND-
Exhibit evidence of at least ONE opioid safety concern (\*indicators of opioid safety concerns described below).
Opioid safety concerns for inclusion purposes include:
moderate-to-high dose opioid prescription (morphine equivalent daily dose \>60mg)
comorbid conditions that increase the risk of opioids including chronic pulmonary disease (e.g., emphysema, chronic bronchitis, asthma, or other breathing problems), sleep apnea, chronic kidney disease, chronic hepatitis or cirrhosis
active high-risk co-prescriptions, including benzodiazepine prescription (any dose of long-term treatment), gabapentin prescription (1800mg or higher) or pregabalin prescription (150mg or higher)
risk of substance use and/or potential opioid misuse as evidenced by unexpected urine toxicology findings in past 6-months OR any documented active substance use disorder (other than tobacco or caffeine) as evidenced by at least 2 encounters within the previous 12-months with a substance use disorder diagnosis.
a positive TAPS score
a positive AUDIT-C score
presence of any adverse events as measured by the adverse effects checklist administered during screening
reported score of \>8 as measured by the Prescribed Opioids Difficulties Scale (PODS).

Exclusion Criteria

Moderate to severe cognitive impairment as measured by the Blessed Orientation Memory Concentration (BOMC) screening tool. -OR-
Current/active prescription for buprenorphine or receipt of buprenorphine in the previous 6-months. -OR-
Inability to read or understand English. -OR-
Severely impaired hearing or speech that would preclude participation in telephone interviews or appointments with the Whole Health Coach. -OR-
Terminal illness/disease with a prognosis of \<12 months. -OR-
Planned move/relocation outside of the treatment areas of the participating enrolling study sites. -OR-
Participants actively working with a Whole Health Coach or who have worked with a Whole Health Coach in the 6-months prior to enrollment. -OR-
Major surgical procedure planned during the study treatment or follow-up period. -OR-
a recent suicide attempt, defined as documented and/or reported suicide attempt within 90 days of the screening date.

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 Birmingham?

Yes, this clinical trial (NCT07149870) has an active research site in Birmingham, AL 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.

Chronic Pain Treatment Options in Birmingham, AL

If you're searching for chronic pain treatment options in Birmingham, AL, this clinical trial (NCT07149870) 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 Birmingham research site is actively enrolling participants for this clinical trial. You'll receive care from experienced chronic pain 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 chronic pain clinical trials near you to find additional studies recruiting in your area.

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Secure · Expert Care · Birmingham, AL