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Love Together, Parent Together (L2P2) for Parental Conflict (L2P2 Trial)

N/A

Waitlist Available

Led By Heather Prime, PhD

Research Sponsored by York University

Eligibility Criteria Checklist

Specific guidelines that determine who can or cannot participate in a clinical trial

Must have

Be older than 18 years old

Timeline

Screening 3 weeks

Treatment Varies

Follow Up week 5-22

Awards & highlights

L2P2 Trial Summary

This trial is a study to test the feasibility of an intervention program to help reduce stress and conflict for couples with young children during the COVID-19 pandemic.

Eligible Conditions

Parental Conflict
Marital Conflict
Marital Relationships
Internet-Based Intervention
Family Conflict

L2P2 Trial Timeline

Screening ~ 3 weeks3 visits

Treatment ~ Varies

Follow Up ~ week 5-22

Screening ~ 3 weeks

Treatment ~ Varies

Follow Up ~week 5-22

This trial's timeline: 3 weeks for screening, Varies for treatment, and week 5-22 for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.

Primary outcome measures

Acceptability

Adherence

Adverse Childhood Experiences

+11 more

Secondary outcome measures

Brief Coparenting Assessment

Child Development

Child Effortful Control

+11 more

L2P2 Trial Design

2Treatment groups

Experimental Treatment

Active Control

Group I: Love Together, Parent Together InterventionExperimental Treatment1 Intervention

Participants will take part in a 3-session writing intervention over the course of 12-week. They will complete a fact-based summary of a recent conflict and answer questions on conflict/conflict-related distress. Next, they will be asked to complete a 9-minute writing task where they reappraise the conflict they previously reported. First, they will watch an instructional video of how to engage in the writing task, by providing definitions and examples of potentially useful conflict reappraisal strategies. Writing prompts include: "… Think about this disagreement … from the perspective of a neutral third party who wants the best for all involved…"; "…what obstacles do you face in trying to take this perspective…?";"… How might you be most successful in taking this perspective … over the next 2 weeks?" Participants in the intervention group will receive emails to prompt use of the reappraisal strategy between writing sessions.

Group II: Wait-List Control GroupActive Control1 Intervention

Participants will take part in a waitlist control group. They will participate in the same number of assessment/sessions as the experimental group. In the sessions that correspond to the intervention (one session every 4 weeks over the course of 12 weeks as in the intervention group), the waitlist group will complete a basic writing task (identical to the intervention group, wherein they provide a fact-based summary of a recent conflict) and they will complete questions regarding conflict history and conflict-related distress. No other writing tasks will take place. Following the 3-month assessment, they will be offered the writing intervention.

Do I qualify?Apply below to find out

Find a Location

Who is running the clinical trial?

York UniversityLead Sponsor

58 Previous Clinical Trials

17,236 Total Patients Enrolled

University of TorontoOTHER

689 Previous Clinical Trials

1,018,403 Total Patients Enrolled

McMaster UniversityOTHER

880 Previous Clinical Trials

2,597,588 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Are there currently any open registrations for this trial?

"According to clinicaltrials.gov, this research is currently seeking participants. The trial was first shared on April 1st 2022 and had its last edit on July 11th 2022."

Answered by AI

What is the cap on participants for this experiment?

"Indeed, research hosted on clinicaltrials.gov discloses that this medical trial is actively seeking participants. This investigation was initially announced on April 1st 2022 and has since been updated July 11th 2022. The study requires the enrollment of 240 patients from a single location."

Answered by AI

What is the aspiration of this experiment?

"This clinical trial's primary objective, which will be monitored between Week 5 and 22, is to understand the effects of COVID on coping. Other secondary objectives include assessing Perceived Partner Responsiveness (scale 8-40 with higher scores being better outcomes), Child Effortful Control (0-84 with higher scores indicating better outcomes), as well as gauging Emotional/Behavioural Problems in patients aged 3 months - 7 years old(Baby Pediatric Symptom Checklist 0-26; Preschool PSC 17: 0-36; Standard PSC 17: 0-34). All these scales have a high score representing improved"

Answered by AI

Recent research and studies

clinicaltrials.govStudy

Love Together, Parent Together: A Protocol for a Pilot Study of an Intervention for Interparental Couples With Young Children

Heather Prime 2022. "Love Together, Parent Together: A Protocol for a Pilot Study of an Intervention for Interparental Couples With Young Children". ClinicalTrials.gov. https://clinicaltrials.gov/ct2/show/NCT05261022.