Mindfulness and Romantic Relationship Quality

NCT ID: NCT04177836

Last Updated: 2024-02-06

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

PHASE1

Total Enrollment

274 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-11-04

Study Completion Date

2024-06-30

Brief Summary

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The overarching aim of this proposal is to experimentally test whether a mindfulness intervention improves relationship quality. Romantic couples from the community will be randomly assigned to one of two arms: mindfulness vs. active control. Both interventions will be completed on a smart-phone for 14 days using identical intervention activities as our existing published research. After the 14-day period, couples will attend a lab visit and provide relationship quality data.

Detailed Description

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Romantic couples from the community will be randomly assigned to one of two arms: mindfulness vs. active control. Thus, both partners will either complete the mindfulness intervention (developed to increase attention towards and acceptance of current experiences) or a relaxation-based active treatment comparison intervention (developed to parallel the structure of the mindfulness intervention without the attention towards or acceptance of present experiences). Both interventions will be completed on a smart-phone for 14 days using identical intervention activities as our existing published research, which demonstrated that the mindfulness intervention reduced stress reactivity and improved daily well-being. After the 14-day period, couples will attend a lab visit and provide multi-method relationship quality data.

Conditions

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The Focus of the Study is Romantic Relationship Quality

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

There are 2 arms to this intervention - mindfulness and active control.
Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

SINGLE

Participants
The participant and the people interacting with participants will be blind to condition.

Study Groups

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MIndfulness

This arm was developed to increase attention towards and acceptance of current experiences.

Group Type EXPERIMENTAL

Mindfulness intervention

Intervention Type BEHAVIORAL

Participants will either complete a mindfulness intervention or active control for 2 weeks on their smartphone

Active Control

This arm is a relaxation-based active treatment comparison intervention, developed to parallel the structure of the mindfulness intervention without the attention towards or acceptance of present experiences.

Group Type ACTIVE_COMPARATOR

Mindfulness intervention

Intervention Type BEHAVIORAL

Participants will either complete a mindfulness intervention or active control for 2 weeks on their smartphone

Interventions

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Mindfulness intervention

Participants will either complete a mindfulness intervention or active control for 2 weeks on their smartphone

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Couples living together for at least 2 years
* Both partners must be fluent in English
* Both partners cannot already engage in regular systematic mind-body practice (\>2 times per week).
* Both partners must have daily access to an internet-enabled smartphone to complete the intervention

Exclusion Criteria

\-
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Carnegie Mellon University

OTHER

Sponsor Role collaborator

University of Delaware

OTHER

Sponsor Role lead

Responsible Party

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Lisa Jaremka

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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University of Delaware

Newark, Delaware, United States

Site Status RECRUITING

Countries

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United States

Central Contacts

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Marcia Ellis

Role: CONTACT

302-831-4591

Lisa Jaremka, PhD

Role: CONTACT

3028314810

Facility Contacts

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Marcia Ellis

Role: primary

302-831-4591

Lisa Jaremka, PhD

Role: backup

3028314810

Other Identifiers

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1R21AT010515-01

Identifier Type: NIH

Identifier Source: org_study_id

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