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NCT07159633 · OurRelationship

OurRelationship-S: A Digital Relationship-Strengthening Program for Couples Experiencing Substance Misuse

What this study is about

This study tests the effectiveness of an online relationship program that has been tailored for couples in which one or both members are in recovery from substance misuse. The purpose of this program is to strengthen the romantic relationship and improve individual functioning.

View original scientific description

This study tests the effectiveness of an online relationship program that has been tailored for couples in which one or both members are in recovery from substance misuse. The purpose of this program is to strengthen the romantic relationship and improve individual functioning. Couples participate in approximately 8 hours of digital content (on their phone or computer) and have a total of five calls with a project coach. Couples will be asked to complete online surveys before and after the program and are paid $200 per couple ($100 per individual) for doing so.

Who can participate

This study lists these criteria on ClinicalTrials.gov. A study coordinator reviews eligibility during screening — this page does not determine whether you qualify.

Inclusion criteria

  • To be eligible to participate, couples will need to be:
  • in a romantic relationship and married, engaged, cohabiting, or dating exclusively for \>6mo;
  • Both partners are willing to participate in the study
  • Both partners are fluent readers of the English language and
  • One or both members of the couple are currently in treatment or recovery services for substance use-related issues.

Exclusion criteria

  • Severe domestic violence: We will utilize exclusion criteria for domestic violence that we have used for the last seven years of OurRelationship services with low-income and military couples. These criteria were developed in consultation with CEO of the National Resource Center on Domestic Violence and several members of the Domestic Violence Hotline. Through these conversations, we concluded it would be appropriate if couples were excluded from OurRelationship services if either person reports in the past 6 months that their partner: 1) Choked me 2) Repeatedly punched me during a fight or beat me up 3) Threatened me with (or used) a gun or knife, or 4) Physically forced me to have sex when I didn't want to. Finally, couples will be excluded if either person reports in the past 6 months that: 5) he/she was "quite afraid", "very afraid", or "extremely afraid" that their partners would physically hurt them during an argument.
  • Inadequate internet connection. To ensure that the program can function properly, participants will be required to have access to high-speed internet in their homes or on their smartphones (with regular wireless/hotspot or a minimum 4G cellular connection).
  • Have already decided to end the relationship. Because the tested programs are designed to help couples improve their relationships (rather than deal with a separation or divorce), couples will be excluded if either partner endorses that they "will probably end my relationship even if it does get better" or that they "have already made the decision to end my relationship."

Where

  • Marietta, Georgia
  • Elkton, Maryland
  • Potsdam, New York
  • Lexington, South Carolina
  • Coppell, Texas

Frequently asked questions

What is a clinical trial?

A clinical trial is a research study that tests new medical treatments, drugs, devices, or procedures to determine their safety and effectiveness. Trials are carefully designed and monitored to protect participants while advancing medical knowledge.

Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. Trials must be reviewed and approved, and participants are closely monitored by medical professionals throughout the study. You can withdraw at any time if you choose.

Will I be compensated?

Many clinical trials offer compensation for your time, travel expenses, and inconvenience. The specific compensation varies by study and will be discussed during the screening process. All study-related medical care is typically provided at no cost to participants.

Will I receive a placebo instead of treatment?

When effective treatment exists, participants typically receive either the standard treatment plus the study intervention, or the standard treatment plus placebo. You would not be denied effective care. Placebos are primarily used when no proven treatment is available, or in addition to standard care. Your trial consent form will clearly explain what treatments you may receive.

Can I leave a trial if I change my mind?

Absolutely. Participation in clinical trials is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty or loss of benefits to which you are otherwise entitled.

How long does a clinical trial last?

Trial duration varies widely depending on the study design and purpose. Some trials last just a few weeks, while others may continue for months or years. The study coordinator will provide specific timeline information during your screening call.

Data: ClinicalTrials.gov · synced Sep 8, 2025 · Source of record for eligibility and locations

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1 of 120 participants interested
1% interest

See if this study fits

A short prescreen based on this study's listed criteria. A coordinator confirms eligibility — this is not a medical assessment.

Preparing your pre-screening questions…

Study locations

Choose your preferred location, or select flexible during enrollment.

RECRUITING

Marietta

Georgia

Location available
RECRUITING

Elkton

Maryland

Location available
RECRUITING

Potsdam

New York

Location available
RECRUITING

Lexington

South Carolina

Location available
RECRUITING

Coppell

Texas

Location available

Express your interest

Share your contact details and a study coordinator can follow up about screening.

Secure & Confidential

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

What participation can include

  • Study-related care provided by the research team
  • Close monitoring by medical professionals
  • Possible compensation for time and travel*
  • The option to withdraw at any time
  • Contributing to medical research that may help future patients

*Compensation varies by study. Confirm details with coordinator.

Typical next steps

  1. 1.Submit this form
  2. 2.Phone screening
  3. 3.In-person assessment if eligible
  4. 4.Begin participation

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Looking for Relationship Conflict Treatment in Marietta?

Join others in Georgia exploring innovative treatment options through clinical research

Relationship Conflict Treatment Options in Marietta, Georgia

If you're searching for Relationship Conflict treatment in Marietta, participating in a clinical research study may provide access to innovative approaches under expert medical supervision. This study is actively recruiting participants in Marietta, Elkton, Potsdam and surrounding areas.

Clinical trials offer participants the opportunity to receive cutting-edge treatments while contributing to medical research that may help future patients with Relationship Conflict. All study-related care is provided at no cost to participants.

Local Sites
3 locations in Georgia
Now Enrolling
Up to 120 participants
Quick Start
Screening available now

Why Consider a Clinical Trial for Relationship Conflict?

Potential Benefits

  • Access to new treatment approaches before public availability
  • Close monitoring by experienced medical professionals
  • Study-related care provided at no cost
  • Contribute to medical research for Relationship Conflict

What to Expect

  • Initial screening to determine eligibility
  • Regular check-ups and monitoring visits
  • Possible compensation for time and travel
  • You can withdraw at any time

Frequently Asked Questions About This Relationship Conflict Study

Important Clinical Trial Information

This information is provided for educational purposes and does not constitute medical advice. Clinical trial participation involves potential risks and benefits. Eligibility requirements apply and will be assessed during the screening process.

Study identifier: NCT07159633. For complete study details, visit ClinicalTrials.gov. Always consult with your healthcare provider before making decisions about your medical care or participating in clinical research.