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Understanding the Psychosocial Needs of Parents Who Have Lost a Child to Cancer

Understanding the Psychosocial Needs of Parents Who Have Lost a Child to Cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00968500
Enrollment
160
Registered
2009-08-31
Start date
2009-08-01
Completion date
2027-06-02
Last updated
2026-04-21

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

Conditions

Parents Who Have Lost a Child to Cancer

Keywords

Grief, bereavement, questionnaires, 09-107

Brief summary

The purpose of this study is to understand the experiences and needs of parents who have lost a child to cancer. This will aid us in developing an intervention that may help parents cope with their loss.

Interventions

Prior to the interview, the measure of prolonged grief disorder symptoms, the PG-13, will be re-administered to participants as a quality assurance check. We will administer 7 self-report measures, which participants can complete in our office, at home, or via telephone, depending on their preferences. These questionnaires should take approximately 75 to 80 minutes to complete. If you are asked to take part in the in-depth interview and you choose to take part, the interview that will take approximately 60 to 90 minutes to complete, depending on the length of the responses to the questions asked. The participant may also be asked if they would be willing to fill out an additional questionnaire about parents' thoughts on the most appropriate timing for raising the topic of a postmortem examination and factors that are important to include in discussions. Despite its importance, autopsy is often not discussed with parents whose child is dying from cancer.

Sponsors

Memorial Sloan Kettering Cancer Center
Lead SponsorOTHER
National Cancer Institute (NCI)
CollaboratorNIH
Dana-Farber Cancer Institute
CollaboratorOTHER
Ohio State University
CollaboratorOTHER
University of Memphis
CollaboratorOTHER
University of Southern California
CollaboratorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

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

Inclusion criteria

* Loss of a child to cancer between 6 months and 6 years ago * Loss of a child between the ages of 6 months and 25 years * Biological or adoptive parent or stepparent * Parent must be age 18 or over * In the judgment of investigators/consenting professionals able to comprehend English to complete study assessments * To be eligible for the qualitative interview, participants more score of 19 or less (\< 19)or 34 or greater (\> 34) on the PG-13 to qualify

Exclusion criteria

* Significant psychiatric disturbance sufficient, in the investigator's judgment, to preclude completion of the assessment measures, interview or informed consent.

Design outcomes

Primary

MeasureTime frame
Identify the unique qualitative themes related to finding meaning among parents who lost a child to cancer to inform development of a conceptually sound meaning-centered grief intervention.2 years

Secondary

MeasureTime frame
Determine differences in qualitative themes of meaning in parents in the high and low Prolonged Grief Disorder subgroups to help select a target population for a meaning-centered grief intervention.2 years
Explore and identify factors associated with bereaved parents' psychosocial service underutilization to guide the development of an acceptable and feasible meaning-centered grief intervention format.2 years

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORRebecca Saracino, PhD

Memorial Sloan Kettering Cancer Center

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 22, 2026