Trialsphere

Benefits For The Patient

Advanced diagnostic testing

Our studies include comprehensive assessments that may not be covered by traditional insurance plans, providing your patients with valuable insights into their health status.

Potential access to investigational products

Participants may receive an innovative treatment that may assist in controlling or improving symptoms related to their condition.

Thorough evaluations and frequent monitoring

Our dedicated research team will closely supervise your patients, helping to identify potential issues or complications before they become more serious.

Around-the-clock support

Our team is available 24/7 to address any concerns or questions that may arise during the study.

Reimbursement and assistance

Eligible participants may receive compensation for their time and effort, as well as travel and transportation assistance.

Voluntary participation

Participation in our studies is entirely voluntary, and your patients may withdraw at any time without any impact on their current care.

Real-time updates for referring providers

As the referring healthcare provider, you will receive regular updates on your patient’s progress throughout the study.

Empower your patients to shape the future of healthcare

By participating in a study, they will make a valuable contribution to medical research—potentially helping countless others facing similar health challenges.

How to
Referring Patients?

Referrals to one of our studies are welcome for patients who may benefit from participation. Eligible participants who enroll after screening will be asked to identify the referring provider, and a referral bonus may be available for qualifying enrollments. Referrals are also welcome for other eligible individuals, including interested friends and family members. After a referral is submitted, our study team will contact the participant, complete a brief screening, and coordinate next steps with them. Research partnerships are welcome, and the team is available to discuss study opportunities.
Disclaimer: Referral bonuses are available for qualifying enrollments and may vary by study.

FAQs

  • Research studies that evaluate the safety and effectiveness of new medications in
    humans
  • Before human testing, these potential treatments undergo rigorous lab animal
    testing to verify safety
  • They are closely regulated by the US Food and Drug Administration (FDA). FDA
    approval is required for new treatments, ensuring they meet stringent quality and
    safety standards before public availability
  • In-depth Healthcare Attention: Benefit from closer health monitoring and personalized care from healthcare professionals throughout the study
  • Access to New Treatments: Gain early access to innovative treatments and contribute to the development of new medical therapies
  • Complimentary Health Assessments: Receive free health screenings, lab tests, imaging, and exams, providing valuable insights into your health
  • Contribute to Medical Advancements: Play a crucial role in advancing medical knowledge and treatments, helping to improve public health
  • Safety and Volunteer Well-being: Enjoy the assurance of a safety-focused environment, with the option to withdraw at any time for your comfort
Yes, however specific requirements and eligibility criteria exist for participating in clinical studies. Here are some key things to keep in mind about who can participate:
  • Age: There are often age minimums and maximums, depending on the study.
  • Health status: To be eligible for the treatment, participants must have the medical condition that the treatment intends to alleviate. There are usually criteria around the type and severity of symptoms. Certain other health conditions may also exclude someone from participating if it could impact results.
  • Gender: Some studies are limited to a single gender, especially early-stage studies testing drugs that interact differently with men vs. women.
  • Prior treatments/therapies: Another criterion often considered is Whether someone has undergone previous treatments related to the condition.
Ultimately, clinical studies set rigorous guidelines on age, health, gender and more. The specifics are narrowed down based on what they want to test and study for any potential new treatment. Getting enrolled can be selective.
Benefits include:
  • Active participation in health care
  • difficult to access and often costly treatments
  • Free testing (i.e. imaging, bloodwork, exams)
  • Assisting others by participating in studies for potential approval and public availability
Participating in a clinical study may carry risks your doctor will disclose. Possible risks of experimental treatment include:
  • Side effects, both known and unknown
  • Study procedures
  • Treatment ineffectiveness
  • Treatment is not practical for all patients
Some clinical studies give patients a placebo instead of experimental treatment. Along with the risks above, the study may need time and attention from participants, including trips to the research location, more treatments, hospital stays, or complex dosage requirements.
Participating in a legitimate clinical study is free, and clinical studies do not require you to have health insurance in order to take part. While every effort is made to ensure that study-related costs are covered by the sponsor, unforeseen expenses may arise. For instance, if you experience side effects that require medical attention outside the study protocol, these costs may not be covered by the study. You are encouraged to discuss any questions or concerns with your health insurance provider and the research team before enrolling in the study

Individuals who participate in clinical studies may receive compensation for their involvement. Compensation is provided for the time and effort outlined in the informed consent form, and the amounts can vary based on study length, required procedures, and participant needs. The sponsor sets the compensation amounts.

Studies may also offer free medical checks, laboratory tests, and study medications.

The current compensation system is not intended to incentivize taking personal risks, and any pressure to participate for payment is against ethical standards. Before enrolling in a study, the research site will disclose the compensation available for time and travel. Compensation should never be the main reason for participation; the primary goal should be helping to advance medical research.

All potential volunteers should learn as much as possible about their disease and the clinical study they are considering. Participants are encouraged to ask questions of the research staff about the study, the care they can expect while participating, and the potential risks. The following questions may be helpful to discuss with the research team before enrolling:
  • What is the purpose of the study?
  • Why do the researchers believe the experimental treatment will be effective?
  • Has the treatment been tested previously?
  • What types of tests and experimental therapies will be used?
  • How do the study’s potential risks, side effects, and benefits compare to my current treatment?
  • How will my illness and the effectiveness of the treatment be tracked during the study?
  • How will this study affect my daily life?
  • How long will the study last?
  • Who will pay for the experimental treatment and other study-related costs?
  • Will I be compensated for my time, travel, or any additional expenses?
  • Will I receive the study results, and if so, when?
  • Who will be responsible for my healthcare during the study?
  • Whom should I contact on the study team if I have questions or concerns during participation?
Discover answers to more frequently asked questions.
Learn More














    Quick Contact

    For referrals or study questions, contact TrialSphere Clinical Research directly:

    FAQs

    Everything you need to know

    • Research studies that evaluate the safety and effectiveness of new medications in humans.
    • Before human testing, these potential treatments undergo rigorous lab animal testing to verify safety.
    • They are closely regulated by the US Food and Drug Administration (FDA). FDA approval is required for new treatments, ensuring they meet stringent quality and safety standards before public availability
    • In-depth Healthcare Attention: Benefit from closer health monitoring and personalized care from healthcare professionals throughout the trial.
    • Access to New Treatments: Gain early access to innovative treatments and contribute to the development of new medical therapies.
    • Complimentary Health Assessments: Receive free health screenings, lab tests, imaging, and exams, providing valuable insights into your health.
    • Contribute to Medical Advancements: Play a crucial role in advancing medical knowledge and treatments, helping to improve public health.
    • Safety and Volunteer Well-being: Enjoy the assurance of a safety-focused environment, with the option to withdraw at any time for your comfort.
    yes however, specific requirements and eligibility criteria exist for participating in clinical trials. Here are some key things to keep in mind about who can participate:
    • Age: There are often age minimums and maximums, depending on the study.
    • Health status: To be eligible for the treatment, participants must have the medical condition that the treatment intends to alleviate. There are usually criteria around the type and severity of symptoms. Certain other health conditions may also exclude someone from participating if it could impact results.
    • Gender: Some trials are limited to a single gender, especially early-stage trials testing drugs that interact differently with men vs. women.
    • Prior treatments/therapies: Another criterion often considered is Whether someone has undergone previous treatments related to the condition.
    Ultimately, clinical trials set rigorous guidelines on age, health, gender and more. The specifics are narrowed down based on what they want to test and study for any potential new treatment. Getting enrolled can be selective.
    Benefits include:
    • Active participation in health care.
    • difficult to access and often costly treatments.
    • Free testing (i.e. imaging, bloodwork, exams).
    • Assisting others by participating in trials for potential approval and public availability.
    Participating in a clinical trial may carry risks your doctor will disclose. Possible risks of experimental treatment include:
    • Side effects, both known and unknown.
    • Study procedures.
    • Treatment ineffectiveness.
    • Treatment is not practical for all patients.
    Some clinical trials give patients a placebo instead of experimental treatment. Along with the risks above, the trial may need time and attention from participants, including trips to the research location, more treatments, hospital stays, or complex dosage requirements.
    Participating in a legitimate clinical trial is free. While every effort is made to ensure that study-related costs are covered by the sponsor, unforeseen expenses may arise. For instance, if you experience side effects that require medical attention outside the study protocol, these costs may not be covered by the study. You are encouraged to discuss any concerns with your health insurance provider the research team before enrolling in the study.
    Individuals who participate in numerous clinical studies receive compensation for their involvement. Some important things to know about compensation:
    • Compensation is for the time and effort outlined and specified in the informed consent compensation amounts vary based on study length, required processes, and participant needs. The sponsor sets the amounts for these compensations.
    • Studies also offer free medical checks, lab tests, and medicines.
    The current compensation system does not incentivize taking personal risks. Such pressure is against ethical standards. Before enrolling in a trial, the research site will disclose compensations for time and travel. Compensation should never be the main reason for participation; the primary goal should be advancing medical study.
    All potential volunteers must learn as much as possible about their disease and the clinical study they are pursuing. Participants should ask members of the study team questions about the trial, the care they can expect while participating, and the potential risks. Participants are encouraged to ask the trial’s study team the following questions:
    • What is the purpose of the trial?
    • Why do the researchers feel the experimental treatment will be effective?
    • Has it been tested previously?
    • What types of tests and experimental therapies are used?
    • How do the research’s potential risks, side effects, and benefits compare to my present treatment?
    • How will my illness and the effectiveness of the treatment be tracked?
    • How will this trial affect my daily life?
    • How long will the trial be?
    • Who will pay for the experimental treatment?
    • Will I get compensated for additional expenses?
    • Will I receive the trial results? When?
    • Who will be in control of my healthcare?
    Discover answers to more frequently asked questions.
    Learn More

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      There are several ways providers can get involved with TrialSphere Clinical Research. Upcoming educational and community events are listed on the Home page and offer a welcoming way to learn more about current and future studies. Questions about provider participation, patient referrals, or research partnerships can be submitted through the Contact Us page.

      For study-specific questions, the Ask An Expert MailChimp form is available. Social media channels provide an easy way to stay connected with updates, announcements, and new research opportunities, and the Newsletter sign-up option delivers periodic study updates directly to inboxes. We always respect your privacy.

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