ClinicalTrials.gg
Not yet recruitingNCT07418320G2T2Updated Feb 18, 2026

Grow Together, Thrive Together: A Feasibility Study of a Brief Relationship Intervention for Emerging Adults and Their Caregivers

An interventional study of Grow Together Thrive Together (G2T2) in Parent Child Relationship, Interpersonal Relations and Young Adults, sponsored by York University. Not yet recruiting at 1 site in Canada. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-02-18.

Sponsored by York University · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

Background. Emerging adulthood is a period of major change in young people's lives, including increased independence, new responsibilities, and shifting relationships with parents or caregivers. During this time, disagreements between emerging adults and caregivers are common and may become more frequent or emotionally intense. How families manage these disagreements may affect relationship quality and emotional well-being for both emerging adults and caregivers. However, there are few brief, accessible programs designed to support emerging adults and caregivers together during this transition.

Grow Together, Thrive Together (G2T2) is a brief, online, writing-based relationship program designed for emerging adults and their caregivers. The program encourages participants to reflect on disagreements using a neutral, outside-observer perspective, with the goal of helping families approach conflict in healthier ways. G2T2 is designed to be low-intensity, self-directed, and accessible, and can be completed remotely using secure online platforms.

The purpose of this study is to evaluate the feasibility and acceptability of the G2T2 program and study procedures, rather than to test effectiveness. This feasibility clinical trial will examine whether emerging adult-caregiver dyads can be successfully recruited and retained, whether participants complete the writing sessions as planned, and whether participants find the program acceptable, easy to use, and understandable. The study will also explore whether participants report using the conflict reappraisal strategy outside of the writing sessions and examine changes in relationship and conflict-related outcomes before and after the program to inform future research.

Participants will take part as emerging adult-caregiver pairs. Each participant will complete an online baseline survey, three brief online writing sessions completed over approximately nine weeks, and a follow-up survey one week after the final session. Each writing session includes brief questions about recent disagreements, a short instructional video, brief questions to check understanding of the strategy, and guided writing exercises focused on reflecting on disagreements and planning how to use the strategy in future interactions. All activities are completed independently and online. Findings from this study will be used to refine the G2T2 program and study procedures and to inform the design of a future, larger randomized controlled trial.

02

Conditions studied

  • Parent Child Relationship
  • Interpersonal Relations
  • Young Adults

Keywords

  • Parent-Child Relations
  • Interpersonal Relations
  • Family Relations
  • Primary Prevention
  • Health Promotion
  • Emerging Adulthood
03

In context

Lead sponsor

York University is the lead sponsor of 51 studies on the registry; 12 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Emerging adults aged 18-25 years and their primary caregiver or parent, enrolled as emerging adult-caregiver dyads
  • Both members of the dyad must independently provide prior to participation
  • Sufficient English literacy to complete online questionnaires in English
  • Reliable access to the internet via a computer or mobile device
  • Dyad members may live together or separately
  • Participants may continue usual or recommended mental health care (e.g., psychotherapy, pharmacotherapy) during the study

Exclusion criteria

Exclusion Criteria:

  • Concurrent participation in a structured family-based intervention (e.g., manualized family therapy or family skills programs) during the study period
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
60 participants (estimated)

Study arms

  • Experimental
    Grow Together, Thrive Together (G2T2) Intervention

    The Grow Together, Thrive Together (G2T2) intervention is a brief, online, self-directed, writing-based relationship intervention for emerging adult-caregiver dyads. Each member of the dyad independently completes three guided writing sessions over approximately nine weeks. Sessions include brief questionnaires assessing recent conflict frequency and distress, a short instructional video introducing a neutral, third-party perspective on conflict, and a brief set of multiple-choice learning check questions to assess understanding of the conflict reappraisal strategy. Participants then complete structured writing prompts that encourage conflict reappraisal, reflection on barriers to strategy use, and planning for applying the strategy in future interactions. Participants also receive brief email or SMS reminders between sessions to encourage practice of the strategy. All study procedures are delivered remotely via secure online platforms.

    Behavioral: Grow Together Thrive Together (G2T2)

Interventions

  • BehavioralGrow Together Thrive Together (G2T2)

    Grow Together, Thrive Together (G2T2) is a brief, online, writing-based relationship intervention designed for emerging adult-caregiver dyads. The intervention is grounded in conflict reappraisal and third-party perspective-taking and aims to reduce negative reciprocity during disagreements by helping participants reinterpret conflicts from a neutral, outside-observer perspective. Across sessions, participants are guided through structured writing exercises that focus on describing recent disagreements factually, considering alternative interpretations of the conflict, identifying barriers to applying the strategy, and planning how to use the reappraisal approach in future interactions. Instructional video content and brief learning check questions support understanding of the core strategy. The intervention is designed to be low-intensity, scalable, and culturally responsive, and is adapted from an evidence-informed writing intervention previously tested in other relational contexts.

06

What researchers measure

Primary outcomes

  1. Recruitment Feasibility

    Recruitment feasibility will be assessed by the proportion of the target sample of emerging adult-caregiver dyads successfully recruited during the planned recruitment period (58 weeks from March 20 2026 to May 1 2027). Feasibility will be evaluated against a predefined success criterion of recruiting at least 70% of the target sample.

    Time frame: Week 0-58

  2. Caregiver Socioeconomic Status (Income and Education)

    Percentage of caregivers meeting socioeconomic criteria, defined as having a household income below the Toronto median and/or a high school education or less. Feasibility will be evaluated against a predefined benchmark of ≥30% of caregivers meeting these criteria.

    Time frame: Week 0

  3. Participant Retention

    Participant retention will be assessed as the proportion of enrolled emerging adult-caregiver dyads who complete the post-intervention assessment one week after the final writing session. Feasibility will be evaluated against a predefined success criterion of at least 75% dyad retention.

    Time frame: Week 0-10

  4. Intervention Adherence

    Intervention adherence will be assessed as the proportion of emerging adult-caregiver dyads who complete at least two of the three online writing sessions. Feasibility will be evaluated against a predefined success criterion of at least 75% adherence.

    Time frame: Week 1-9

  5. Intervention Uptake

    Intervention uptake will be assessed as the proportion of emerging adult-caregiver dyads reporting use of the conflict reappraisal strategy since their previous intervention session. Feasibility will be evaluated against a predefined success criterion of at least 80% uptake.

    Time frame: Week 5-10

  6. Intervention Acceptability

    Intervention acceptability will be assessed using participant responses to a validated acceptability questionnaire based on the Theoretical Framework of Acceptability. Acceptability will be evaluated as the proportion of participants endorsing at least "agree" on 80% or more of questionnaire items, with a predefined success criterion of at least 80%.

    Time frame: Week 10

  7. Digital Usability

    Digital usability will be assessed using participant ratings on the Ease of Use and Comprehension subscales of the Website Evaluation Questionnaire. Usability will be evaluated as the proportion of participants endorsing at least "agree" on 80% or more of items, with a predefined success criterion of at least 80%.

    Time frame: Week 10

  8. Racial Diversity

    Percentage of participants identifying as racialized. Feasibility will be evaluated against a predefined benchmark of ≥55.7% racialized participants.

    Time frame: Week 0

  9. Sexual and Gender Diversity

    Percentage of emerging adult participants identifying as Two-Spirit, lesbian, gay, bisexual, transgender, queer, or other sexual and/or gender minority identities (2SLGBTQ+). Feasibility will be evaluated against a predefined benchmark of ≥10.5% 2SLGBTQ+ emerging adults.

    Time frame: Week 0

  10. Immigrant Status

    Percentage of participants who are foreign-born. Feasibility will be evaluated against a predefined benchmark of ≥46.6% foreign-born participants.

    Time frame: Week 0

Secondary outcomes

  1. Change in Emerging Adult-Caregiver Relationship Quality

    Relationship quality will be assessed using the Parental Environment Questionnaire (PEQ; caregiver and emerging adult versions), which includes five subscales: conflict, involvement, regard for parent, regard for child, and structure. Exploratory analyses will examine mean change from baseline to one week post-intervention.

    Time frame: Pre-post change from Week 0 to Week 10

  2. Change in Conflict Behavior

    Conflict behavior will be assessed using the 20-item Conflict Behavior Questionnaire (CBQ-20; caregiver and emerging adult versions). Exploratory analyses will examine pre-post changes in reported conflict behaviors from baseline to one week post-intervention.

    Time frame: Pre-post change from Week 0 to Week 10

  3. Change in Emerging Adult Support-Seeking and Perceived Support

    Emerging adult support-seeking behaviors and perceptions of support received from caregivers will be assessed using two five-item self-report scales completed by emerging adults. The scales assess the frequency and perceived quality of support-seeking behaviors and caregiver support responses. Exploratory analyses will examine pre-post change from baseline to one week post-intervention.

    Time frame: Pre-post change from Week 0 to Week 10

  4. Change in Conflict-Related Distress

    Conflict-related distress will be assessed using two self-report items following each fact-based conflict summary assessing distress related to caregiver or emerging adult behavior during conflicts. Exploratory analyses will examine change from baseline to one week post-intervention.

    Time frame: Pre-post change from Week 0 to Week 10

  5. Change in Parental Autonomy Support

    Parental autonomy-support will be assessed using caregiver- and emerging adult-report measures assessing autonomy-supportive parenting behaviors. Exploratory analyses will examine pre-post change in parental autonomy-support from baseline to one week post-intervention.

    Time frame: Pre-post change from Week 0 to Week 10

07

Study locations

1 site
  • York University
    North York, Ontario M3J 1P3, Canada
    • Heather Prime, PhD · Contacthprime@yorku.ca · 416-736-5117
    • Parker Grant, HBSc · Contactparkerg@yorku.ca · 780-983-9996
    • Heather Prime, PhD · Principal investigator
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 18, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07418320
Lead sponsor
York University
Responsible party
Heather Prime (Associate Professor in the Department of Psychology, York University, York University) — Principal investigator
First posted
Feb 18, 2026
Start date
Mar 20, 2026 (estimated)
Primary completion
May 1, 2027 (estimated)
Completion
May 31, 2027 (estimated)
Last update
Feb 18, 2026

Study contacts

Heather Prime, PhD
Contact
hprime@yorku.ca
416-736-5117
Parker Grant, HBSc
Contact
parkerg@yorku.ca
780-983-9996
Heather Prime, PhD
principal investigator · York University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Feb 2026. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion