Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06872840

Adapting The Fear Of Recurrence Therapy (FORT) for Parents and Establishing Acceptability and Feasibility

Led by University of Ottawa · Updated on 2025-09-22

36

Participants Needed

1

Research Sites

91 weeks

Total Duration

On this page

Sponsors

U

University of Ottawa

Lead Sponsor

C

Children's Hospital of Eastern Ontario

Collaborating Sponsor

AI-Summary

What this Trial Is About

Clinical levels of fear of cancer recurrence (FCR) affect up to 59% of adult cancer survivors. Family caregivers experience equal or greater levels of FCR, which has been linked to lower quality of life and increased distress. FCR can be addressed in cancer survivors with brief interventions. However, none of these interventions have been tested with parents of childhood cancer survivors. This is an urgent gap: the survival rates of childhood cancer have increased more rapidly than for adult cancers, resulting in a growing population of childhood cancer survivors who, along with their families, need support. The goals of this pilot study are to demonstrate 1) that a newly adapted intervention of FORT (Parent-FORT) is feasible (i.e., participant recruitment, attendance and participation) and acceptable (i.e., parent satisfaction of the intervention) for a larger study, and 2) the clinical implications of Parent-FORT on fear of cancer recurrence (FCR) and quality of life in parents of childhood cancer survivors. Parents will be randomly assigned to participate in the Parent-FORT intervention immediately or a three-month waitlist control group. They will complete a questionnaire package before and after the intervention, as well as at a three month follow up. This study will help bridge an important gap in bringing evidence-based care to parents who have never been offered help before for their FCR.

CONDITIONS

Official Title

Adapting The Fear Of Recurrence Therapy (FORT) for Parents and Establishing Acceptability and Feasibility

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Parent or primary caregiver of a childhood cancer survivor under 18 years of age
  • Child is at least 1 month from completing active treatment with no cancer recurrence
  • Fear of Cancer Recurrence Inventory-Short Form-Parent version score of 13 or greater
  • Access to a computer and internet connection
  • Living in Canada
Not Eligible

You will not qualify if you...

  • Parent of a pediatric cancer survivor who is 18 years or older
  • Parent of a child who had hematopoietic cell transplantation and has active chronic or acute graft-versus-host disease not stabilized for at least 3 months
  • Non-English speaking
  • Currently participating in another therapist-led psychosocial therapy group
  • Parent with unmanaged or undermanaged mental health disorder affecting group work
  • More than one parent/caregiver per child cannot participate

AI-Screening

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Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Ottawa

Ottawa, Ontario, Canada, K1N6N5

Actively Recruiting

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Research Team

C

Celeste Holy, B.A

CONTACT

S

Sophie Lebel, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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