Knoxville, TNNCT07214012Now EnrollingIRB Ready

Short Interpregnancy Intervals Clinical Trial in Knoxville, TN

Access cutting-edge short interpregnancy intervals treatment through this clinical trial at a research site in Knoxville. Study-provided care at no cost to qualified participants.

Sponsored by University of Tennessee Graduate School of Medicine

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Expert Care in Knoxville

Access short interpregnancy intervals specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related short interpregnancy intervals treatment provided free

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Check if you qualify for this short interpregnancy intervals clinical trial in Knoxville, TN

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Why Participate?

  • No-Cost Study Care

  • Local to Knoxville

    Convenient for TN 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 Knoxville site if eligible
  4. 4Begin participation

About This Short Interpregnancy Intervals Study in Knoxville

The goal of this pilot trial is to examine the feasibility and acceptability of the Planning Together protocol The hypothesis of this study are 1. The study will achieve feasibility, demonstrated by ≥80% study accrual (30 couples in 8 months), ≥75% protocol adherence, and ≥75% (e.g., education workbook completion) 2. The intervention will be acceptable, with \>80% of participants reporting satisfaction with Planning Together. 3. Patterns of primary outcomes (contraceptive knowledge, communication quality, community referral utilization) and secondary outcomes (agreed contraceptive plan, consistent contraceptive usage and satisfaction, psychological distress, and Short Interpregnancy Intervals \[SII\]) will suggest benefits of the intervention.

Sponsor: University of Tennessee Graduate School of Medicine

Who Can Participate

Inclusion Criteria

Patient Inclusion Criteria:
\> 20 weeks pregnant, age 18+
The pregnant person has an available romantic partner, and the couple was able to get pregnant on their own or will be able to after the delivery
separately, the pregnant person reports being in a sexually, psychologically and physically safe relationship
English-speaking Romantic Partner Inclusion Criteria:
18 years of age and older
Cohabiting with the patient; in a romantic relationship with patient
Capable of getting the patient pregnant after delivery
Does not need to be the biological father of the current pregnancy
English-speaking (in order to take part in the interview as the interviewer does not speak Spanish)

Exclusion Criteria

Patient Exclusion Criteria:
Participant is under the age of 18
Documented cognitive impairment or psychiatric condition in pregnant person's medical record (e.g., severe learning disability, dementia, current psychotic disorder, suicidality)
Participation in a concurrent contraceptive education intervention
The pregnant person has a high-risk medical condition Romantic Partner Exclusion Criteria:
Less than 18 years of age
Are not cohabiting with the patient; not in a romantic relationship with patient
Not capable of getting the patient pregnant after delivery

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 Knoxville?

Yes, this clinical trial (NCT07214012) has an active research site in Knoxville, TN 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.

Short Interpregnancy Intervals Treatment Options in Knoxville, TN

If you're searching for short interpregnancy intervals treatment options in Knoxville, TN, this clinical trial (NCT07214012) 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 Knoxville research site is actively enrolling participants for this clinical trial. You'll receive care from experienced short interpregnancy intervals 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 short interpregnancy intervals clinical trials near you to find additional studies recruiting in your area.

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