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Love Together, Parent Together: A Feasibility Study

Love Together, Parent Together (L2P2): A Feasibility Study of an Ultra-brief Couples Conflict Program for Parents of Young Children

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05143437
Acronym
L2P2
Enrollment
34
Registered
2021-12-03
Start date
2021-08-26
Completion date
2021-11-14
Last updated
2021-12-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Family Conflict, Internet-Based Intervention

Keywords

Couples' relationships, Family Systems, Writing Intervention, Non-randomised, Feasibility study

Brief summary

The COVID-19 pandemic has introduced additional stressors and challenges to couples' relationships, with potential ripple effects across all family subsystems and child adjustment. Among those who are particularly vulnerable to heightened conflict and lower relationship satisfaction during this time are couples with young children, whose relationships may have already been tenuous prior to the pandemic. The Love Together Parent Together (L2P2) program is a brief, low-intensity writing intervention adapted for parents of young children, designed to reduce conflict-related distress and prevent relationship deterioration. Based on an original writing program by Finkel and colleagues, adaptations include intervention duration and study population. The current study will examine key feasibility metrics related to this adapted intervention program with the goal of identifying problems and informing parameters of future pilot and/or main randomized controlled trials (RCT). The current study is a non-randomised feasibility study, using a single-arm, pre-test/post-test design to primarily assess the feasibility of a large trial, and secondarily to assess the potential effects on outcomes to be used in a future RCT. Couples will be recruited through three community-based agencies with the goal of obtaining a socio-demographically diverse sample. The first 20 couples to enroll will be included. Baseline and post-intervention surveys will be conducted, and a writing intervention will take place (three 7-minute sessions over the course of four weeks). The primary feasibility metrics will include recruitment rates, appropriateness of eligibility criteria, sample diversity, retention, uptake, and adherence, and acceptability. In addition, the researchers will develop an objective primary outcome measure of couple we-ness based on analysis of writing samples. The secondary outcomes will include couples' measures (i.e., relationship quality, perceived partner responsiveness, self-reported partner responsiveness, conflict-related distress), and other family outcomes (i.e., parent-child relations, parental/child mental health, and parenting practices). Criteria for success are outlined and failure to meet criteria will result in adaptations to measurement schedule, intervention design, recruitment approaches, and/or other elements of the study design. This feasibility study will inform several components of the procedures used for a subsequent pilot RCT, which will examine the feasibility of the methodology used to evaluate the program (e.g., randomization, attrition to follow up assessment/across groups, and sample size estimation, preliminary effectiveness), and a main trial, which will investigate the effectiveness of the intervention on primary outcome measures as well as mediating pathways.

Detailed description

See attached protocol.

Interventions

BEHAVIORALLove Together Parent Together

A brief, low-intensity writing intervention adapted for parents of young children, designed to reduce conflict-related distress, prevent relationship deterioration and encourage the use of conflict reappraisal strategies designed to reduce conflict-related distress, etc.

Sponsors

University of Toronto
CollaboratorOTHER
McMaster University
CollaboratorOTHER
York University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Both participants endorse being in a relationship * Both partners reside in the same home * There are one or more children under the age of 6 living at home * Both participants are over age 18 years * Both members of a couple agree to participate

Exclusion criteria

• No current plans or history of separation or divorce as this is meant to be a secondary preventative intervention for couples experiencing some but not severe relationship difficulties.

Design outcomes

Primary

MeasureTime frameDescription
Risk for Relationship Distress - COVID-19 Family StressorsWeek 0The percentage of participants scoring 'high' (\>29) on the COVID-19 Family Stressor Scale. Minimum score=16, maximum score=48. Higher scores correspond to worse outcomes.
AcceptabilityWeek 6Looking for the percentage of participants reporting at least 'good' on 80 % or more indicators on an Implementation Acceptability Scale that will assess attitude, burden, perceived effectiveness, and ethicality. Minimum score=7, maximum score=35. Higher scores correspond to better outcomes.
Participants Enrolled Per WeekWeek 0Number of participants enrolled per week, stratified by recruitment source.
Participant EducationWeek 0The percentage of participants with less than or equal to a high school degree.
Racial DiversityWeek 0The percentage of participants who are a racial minority.
Immigrant StatusWeek 0The percentage of participants who are an immigrant.
Sexual DiversityWeek 0The percentage of participants who are gender and/or sexually diverse.
Risk for Relationship Distress - Dyadic AdjustmentWeek 0The percentage of participants scoring in the 'clinical' range (\>13) on the Dyadic Adjustment Scale. Minimum score=1, maximum score=22. Higher scores correspond to worse outcomes.
Participants Accessed Per WeekWeek 0Number of participants accessed (I.e., initiate registration) per week, stratified by recruitment source.
Couple we-nessWeek 1-5Assessing couple we-ness using a content analysis of writing samples collected during the intervention.
Appropriateness of Eligibility CriteriaWeek 0Percentage of interested participants that meet inclusion criteria (with reasons for exclusion).
Participant IncomeWeek 0The percentage of participants income that is less than or equal to the regional median.
RetentionWeek 6The percentage of participants who remain in study until the end of the post-intervention assessment.
UptakeWeek 3-5The percentage of participants reporting some use of conflict reappraisal outside of sessions.
AdherenceWeek 1-5The percentage of participants who complete 2/3 intervention sessions.

Secondary

MeasureTime frameDescription
Pre-Post Change in Parent-Child RelationsPre-post change from week 0 to week 6.Using the Parenting Practices Scale from the Ontario Child Health Study. Minimum score=11, maximum score=55. Higher scores correspond to better outcomes.
Pre-Post Change in Couples' Relationship QualityPre-post change from week 0 to week 6.Using the Perceived Relationship Quality Scale. Minimum score= 18, maximum score=126. Higher scores correspond to better outcomes.
Pre-Post Change in Conflict-Related NegativityPre-post change from week 0 to week 6.Using two items following fact-based summary: I was angry at my partner for his/her behaviour during this conflict, My partner's behaviour during this conflict was highly upsetting to me. Minimum score=2, maximum score=14. Higher scores correspond to worse outcomes.
Pre-Post Change in Perceived Partner ResponsivenessPre-post change from week 0 to week 6.Using the Perceived Partner Responsiveness-Insensitivity Scale (PRI-R) - Brief Version. Minimum score=8, maximum score=40. Higher scores correspond to better outcomes.
Pre-Post Change in Child Emotional and Behavioural ProblemsPre-post change from week 0 to week 6.Scores will be standardized within each age group and used as a single outcome variable. Using the Pediatric Symptom Checklist (Baby, Preschool, and Standard versions). The Baby Pediatric Symptom Checklist: Minimum score=0, maximum score=26. Higher scores correspond to worse outcomes. The Preschool Pediatric Symptom Checklist (PPSC-17): Minimum score=0, maximum score=36. Higher scores correspond to worse outcomes. The Pediatric Symptom Checklist-17: Minimum score=0, maximum score=34. Higher scores correspond to worse outcomes.
Pre-Post Change in Responsiveness Towards PartnerPre-post change from week 0 to week 6.Using the Perceived Partner Responsiveness-Insensitivity Scale (PRI) - Brief with items flipped to reflect responsiveness towards partner. Minimum score=8, maximum score=40. Higher scores correspond to better outcomes.
Pre-Post Change in Parent Mental HealthPre-post change from week 0 to week 6.Using the Kessler Psychological Distress Scale. Minimum score=10, maximum score=50. Higher scores correspond to worse outcomes.

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 11, 2026