Couples' Affect in Relationships: Testing a Well-Being App for Couples
Official title: Couples' Affect in Relationships Study
Run by University of Wisconsin, Madison · NCT06907654 · Data updated 2026-11-12
We’re testing whether using a well-being mobile program with one partner in a long-term relationship can improve both partners’ happiness and relationship satisfaction.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 2000 (estimated) |
| Sponsor | University of Wisconsin, Madison Academic / other |
| Locations | 1 site (Madison, Wisconsin) |
| Status | Recruiting |
| Started | August 4, 2026 |
| Main results expected | December 2028 |
| Study ends | December 2028 |
| Registry record updated | October 13, 2026 |
| Trial ID | NCT06907654 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults 18 and older in a married, cohabiting, or dating relationship of at least 12 months, who are English-speaking, US citizens or permanent residents, and have a smartphone.
✕Probably not a fit
Individuals with severe IPV risk, active suicidality, psychosis/manic symptoms, prior extensive meditation experience, or previous use of the Healthy Minds Program may not benefit or participate.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study delivers the Healthy Minds Program to one member of a long-term couple and measures relationship satisfaction, distress, well-being, and mindfulness in both partners. The control condition provides a list of well-being resources. Participants complete online surveys about thoughts, feelings, and relationship dynamics at specified intervals. Eligibility includes adults in committed relationships for at least 12 months, English speakers, smartphone users, and adults with mild depressive symptoms. The study is conducted at the University of Wisconsin–Madison and led by UW–Madison researchers.
Why it matters
Potential benefit: If successful, participants could experience improved well-being and better relationship functioning.
How similar studies have gone: Prior studies with digital well-being interventions have shown mixed but promising effects on individual well-being and relationship-related outcomes.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age ≥ 18 years * Be either married, living together, OR in a dating relationship for at least 12 months * Proficiency in English * US citizen or permanent resident * If non-monogamous, must be able to enroll in the study with a primary partner with whom they spend the majority of their time. * Use of a smartphone (primary participant only) * Phone able to receive SMS text messages * Depression symptoms (≥ 5 on PHQ-9; primary participant only) Exclusion Criteria: * Severe physical or sexual relationship aggression during the past 6 months (any item endorsement on 5-item severe IPV screener) * Endorsement of active suicidality * History of psychosis or mania * Prior use of the Healthy Minds Program app * Prior significant experience with meditation * Severe hearing impairment that would interfere with the use of an audio-based intervention (primary participant only) * Did not pass video attention check * Investigators may also track the time it takes for participants to complete surveys and use survey timing as a method to flag for suspicious bot activity * Participant presents false or misleading information or other indicators that the participant may be participating in the study in bad faith. At screening, each participant's address will be checked and they will be excluded if the address is 1) invalid or 2) a non-residential address. Participants will also be excluded if the same email is provided for both partners. Participants will be excluded if they fail the attention check item in the baseline survey. Participants will be excluded if they complete their screeners \<= 20 minutes of each other.
Where it's running
-
University of Wisconsin - Madison
Madison, Wisconsin, United States Recruiting
Study contacts
- Principal investigator: Simon Goldberg, PhD — University of Wisconsin, Madison
- Study coordinator: Lily Smith
- Email: cares@chm.wisc.edu
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Medical and psychiatric profiling of adults admitted to general adult psychiatry wards
This project will collect questionnaires, rating scales, and case-note information from adults admitted to general adult psychiatry wards to see what their physical and mental health profiles look like.
-
Long-term psychotropic medication effects on eye movements measured with the Gaize VR headset
This project will test whether the Gaize VR headset can detect eye-movement patterns associated with long-term use of prescribed psychotropic medications in adults.
-
Psychiatric Symptoms and Quality of Life in Graft-versus-Host Disease
This project will see if psychiatric symptoms like depression are linked to GvHD symptom severity and health-related quality of life in adults with graft-versus-host disease.
-
Digital twins to classify mental health patterns in adults with diabetes
This project will try to create 'digital twin' profiles that combine glucose, mood, and behavior data to track mental health patterns in adults with diabetes.
-
Fluoxetine added to immunotherapy for advanced liver and gallbladder cancer with depression or anxiety
This trial will test whether adding the antidepressant fluoxetine to standard PD-1/PD-L1 immunotherapy helps people with advanced liver or gallbladder cancers who also have depression or anxiety.
-
Teen Recovery: Inspiration, Support, and Empowerment program
This pilot will test whether an online peer-led recovery and support program helps 15–18-year-olds recently discharged from psychiatric care reduce suicidal thoughts, depression, anxiety, and re-hospitalization.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.