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Childhood Cancer Survivors' Knowledge of Diagnosis,Treatment and Risk of Late Effects: Specialized Survivorship Clinic

Childhood Cancer Survivors' Knowledge of Their Diagnosis, Treatment, and Risk of Late Effects: The Impact of Care in a Specialized Survivorship Clinic

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01223872
Enrollment
188
Registered
2010-10-19
Start date
2010-08-31
Completion date
2015-08-31
Last updated
2017-04-04

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

Conditions

Childhood Cancer

Brief summary

This two-part research study will compare childhood cancer survivors receiving specialized follow-up care in the REACH for Survivorship clinic to patients receiving routine follow-up care.

Interventions

OTHERinterview

* Standard Interview (2-15 years from last treatment) * Demographic data interview (pre-initial study interview)

OTHERclinic visit and interview

* REACH Clinic Visit(initial or regular) * Post-REACH Clinic Interview (3mos from initial or regular clinic visit) * Demographic data interview(pre-initial study interview)

OTHERinterviews and clinic visit

* Pre-REACH Clinic Interview(2-15 yrs from last treatment) * REACH Clinic Visit(initial or regular) * Post-REACH Clinic Interview(1mo from initial clinic visit) * Post-REACH Clinic Interview(3mos from initial or regular clinic visit) * Demographic data interview(pre-initial study interview)

Sponsors

Vanderbilt University Medical Center
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
No minimum to 21 Years
Healthy volunteers
No

Inclusion criteria

* Treatment for primary malignancy per risk-adapted protocol * Age ≤ 21 years at time of diagnosis * Currently alive without evidence of disease * Off therapy for no more than 15 years

Exclusion criteria

-Patients who have received a bone marrow transplant

Design outcomes

Primary

MeasureTime frameDescription
Knowledge gained by attending a multispecialty Survivorship Clinic which will be measured by comparison of self report with medical record data in both cross-sectional and longitudinal approach.12 monthsIn addition to data from patient interviews, a review of medical records will include general patient demographic data as well as data regarding cancer diagnosis, treatment and ongoing follow-up care.

Secondary

MeasureTime frameDescription
An analysis of differences in relative levels of recommended screening for late effects that childhood cancer survivors have received based on the type of their long-term follow-up care comparing medical records against Survivorship Care Plan.12 monthsScored responses will allow for quantitative analysis of differences within and between the cohorts of patients
A qualitative evaluation of program feedback will serve to improve the care provided in the REACH for Survivorship clinic12 monthsThis data will be evaluated qualitatively for trends.
Characterizing how the initial consultation in a specialized clinic impacts childhood cancer survivors' knowledge of their cancer diagnosis, treatment, and risk of late effects by comparing patient's understanding among 3 sampled timepoints.pre-clinic and a post-clinic interviews at 1 and 3 months.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026