Trial Outcomes & Findings for Education Tools to Support Pediatric Survivor Care (NCT NCT04257058)
NCT ID: NCT04257058
Last Updated: 2025-05-15
Results Overview
Knowledge was assessed at baseline and 2 weeks post-intervention, with the Survivor Care Knowledge scale, that includes 15-item multiple-choice quiz to assess participants' knowledge of the content covered in the electronic educational materials previously provided. Total score ranges from 0-15. Higher score is associated with better outcome.
COMPLETED
NA
89 participants
Baseline, 2 weeks post-intervention
2025-05-15
Participant Flow
This study and the data presented below only refers to the young adult survivors and does not include parents. Parents were not enrolled in this study. "Participants" refer to young adult cancer survivors.
Participant milestones
| Measure |
Electronic Educational Material
Participants in the trial included young adult survivors of childhood cancer. Participants completed an online pre-test survey via REDCap. After the pre-test is completed, participants review electronic media in REDCap. Study staff confirmed review of material and scheduled a post-test survey to be competed in REDCap two weeks after material is reviewed.
|
|---|---|
|
Overall Study
STARTED
|
89
|
|
Overall Study
COMPLETED
|
58
|
|
Overall Study
NOT COMPLETED
|
31
|
Reasons for withdrawal
| Measure |
Electronic Educational Material
Participants in the trial included young adult survivors of childhood cancer. Participants completed an online pre-test survey via REDCap. After the pre-test is completed, participants review electronic media in REDCap. Study staff confirmed review of material and scheduled a post-test survey to be competed in REDCap two weeks after material is reviewed.
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|---|---|
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Overall Study
Lost to Follow-up
|
31
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Baseline Characteristics
Education Tools to Support Pediatric Survivor Care
Baseline characteristics by cohort
| Measure |
Electronic Educational Material
n=89 Participants
Participants in the trial included young adult survivors of childhood cancer. Participants completed an online pre-test survey via REDCap. After the pre-test is completed, participants review electronic media in REDCap. Study staff confirmed review of material and scheduled a post-test survey to be competed in REDCap two weeks after material is reviewed.
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|---|---|
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Age, Continuous
|
19.8 years
STANDARD_DEVIATION 1.2 • n=5 Participants
|
|
Sex/Gender, Customized
Female
|
41 Participants
n=5 Participants
|
|
Sex/Gender, Customized
Male
|
45 Participants
n=5 Participants
|
|
Sex/Gender, Customized
Non-Binary
|
3 Participants
n=5 Participants
|
|
Ethnicity (NIH/OMB)
Hispanic or Latino
|
26 Participants
n=5 Participants
|
|
Ethnicity (NIH/OMB)
Not Hispanic or Latino
|
63 Participants
n=5 Participants
|
|
Ethnicity (NIH/OMB)
Unknown or Not Reported
|
0 Participants
n=5 Participants
|
|
Race (NIH/OMB)
American Indian or Alaska Native
|
2 Participants
n=5 Participants
|
|
Race (NIH/OMB)
Asian
|
4 Participants
n=5 Participants
|
|
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
|
0 Participants
n=5 Participants
|
|
Race (NIH/OMB)
Black or African American
|
20 Participants
n=5 Participants
|
|
Race (NIH/OMB)
White
|
56 Participants
n=5 Participants
|
|
Race (NIH/OMB)
More than one race
|
3 Participants
n=5 Participants
|
|
Race (NIH/OMB)
Unknown or Not Reported
|
4 Participants
n=5 Participants
|
|
Region of Enrollment
United States
|
89 participants
n=5 Participants
|
PRIMARY outcome
Timeframe: Baseline, 2 weeks post-interventionPopulation: Total number of participants analyzed per time point include participants that completed the corresponding visit and the specific assessment for this study outcome.
Knowledge was assessed at baseline and 2 weeks post-intervention, with the Survivor Care Knowledge scale, that includes 15-item multiple-choice quiz to assess participants' knowledge of the content covered in the electronic educational materials previously provided. Total score ranges from 0-15. Higher score is associated with better outcome.
Outcome measures
| Measure |
Electronic Educational Material
n=89 Participants
Participants in the trial included young adult survivors of childhood cancer. Participants completed an online pre-test survey via REDCap. After the pre-test is completed, participants review electronic media in REDCap. Study staff confirmed review of material and scheduled a post-test survey to be competed in REDCap two weeks after material is reviewed.
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|---|---|
|
Survivor Care Knowledge Scale
Baseline
|
10.6 score on a scale
Standard Deviation 2.1
|
|
Survivor Care Knowledge Scale
2 weeks post-intervention
|
11.2 score on a scale
Standard Deviation 2.3
|
SECONDARY outcome
Timeframe: Baseline, 2 weeks post-interventionPopulation: Total number of participants analyzed per time point include participants that completed the corresponding visit and the specific assessment for this study outcome.
5-item study adapted Champion Benefits Scale for Mammography Screening. Total score ranges from 5-25. Lower score equals fewer perceived benefits of survivor care.
Outcome measures
| Measure |
Electronic Educational Material
n=89 Participants
Participants in the trial included young adult survivors of childhood cancer. Participants completed an online pre-test survey via REDCap. After the pre-test is completed, participants review electronic media in REDCap. Study staff confirmed review of material and scheduled a post-test survey to be competed in REDCap two weeks after material is reviewed.
|
|---|---|
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Benefits for Survivor Care
Baseline
|
12.6 score on a scale
Standard Deviation 1.9
|
|
Benefits for Survivor Care
2 weeks post-intervention
|
12.9 score on a scale
Standard Deviation 1.8
|
SECONDARY outcome
Timeframe: Baseline, 2 weeks post-interventionPopulation: Total number of participants analyzed per time point include participants that completed the corresponding visit and the specific assessment for this study outcome.
11-item study adapted Champion Barriers Scale for Mammography Screening. Total score ranges from 11-55. Lower score equals fewer perceived barriers to survivor care.
Outcome measures
| Measure |
Electronic Educational Material
n=89 Participants
Participants in the trial included young adult survivors of childhood cancer. Participants completed an online pre-test survey via REDCap. After the pre-test is completed, participants review electronic media in REDCap. Study staff confirmed review of material and scheduled a post-test survey to be competed in REDCap two weeks after material is reviewed.
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|---|---|
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Barriers for Survivor Care
Baseline
|
20.2 score on a scale
Standard Deviation 5.9
|
|
Barriers for Survivor Care
2 weeks post-intervention
|
19.9 score on a scale
Standard Deviation 5.3
|
SECONDARY outcome
Timeframe: Baseline, 2 weeks post-interventionPopulation: Total number of participants analyzed per time point include participants that completed the corresponding visit and the specific assessment for this study outcome.
3-item study adapted Champion Susceptibility Scale for Mammography Screening. Total score ranges from 3-15. Lower score equals less susceptibility to late effects of treatment.
Outcome measures
| Measure |
Electronic Educational Material
n=89 Participants
Participants in the trial included young adult survivors of childhood cancer. Participants completed an online pre-test survey via REDCap. After the pre-test is completed, participants review electronic media in REDCap. Study staff confirmed review of material and scheduled a post-test survey to be competed in REDCap two weeks after material is reviewed.
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|---|---|
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Perceived Susceptibility for Late Effects
Baseline
|
9.7 score on a scale
Standard Deviation 3.1
|
|
Perceived Susceptibility for Late Effects
2 weeks post-intervention
|
10.4 score on a scale
Standard Deviation 2.7
|
SECONDARY outcome
Timeframe: Baseline, 2 weeks post-interventionPopulation: Total number of participants analyzed per time point include participants that completed the corresponding visit and the specific assessment for this study outcome.
2-item study adapted Ajzen's Theory of Planned Behavior- Intentions. Total score ranges from 2-14. Lower score equals greater intention to engage in long-term follow-up care.
Outcome measures
| Measure |
Electronic Educational Material
n=89 Participants
Participants in the trial included young adult survivors of childhood cancer. Participants completed an online pre-test survey via REDCap. After the pre-test is completed, participants review electronic media in REDCap. Study staff confirmed review of material and scheduled a post-test survey to be competed in REDCap two weeks after material is reviewed.
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|---|---|
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Intentions for Survivor Care
Baseline
|
11.8 score on a scale
Standard Deviation 3.4
|
|
Intentions for Survivor Care
2 weeks post-intervention
|
11.4 score on a scale
Standard Deviation 3.4
|
SECONDARY outcome
Timeframe: Baseline, 2 weeks post-interventionPopulation: Total number of participants analyzed per time point include participants that completed the corresponding visit and the specific assessment for this study outcome.
8-item Perceived Health Competence Scale (PHCS). Total score ranges from 8-40. Lower score equals lower perceived health competence.
Outcome measures
| Measure |
Electronic Educational Material
n=89 Participants
Participants in the trial included young adult survivors of childhood cancer. Participants completed an online pre-test survey via REDCap. After the pre-test is completed, participants review electronic media in REDCap. Study staff confirmed review of material and scheduled a post-test survey to be competed in REDCap two weeks after material is reviewed.
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|---|---|
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Change in Perceived Health Competence Scale (PHCS)
Baseline
|
28.7 score on a scale
Standard Deviation 5.2
|
|
Change in Perceived Health Competence Scale (PHCS)
2 weeks post-intervention
|
27.0 score on a scale
Standard Deviation 5.6
|
Adverse Events
Electronic Educational Material
Serious adverse events
| Measure |
Electronic Educational Material
n=89 participants at risk
Participants in the trial included young adult survivors of childhood cancer. Participants completed an online pre-test survey via REDCap. After the pre-test is completed, participants review electronic media in REDCap. Study staff confirmed review of material and scheduled a post-test survey to be competed in REDCap two weeks after material is reviewed.
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|---|---|
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Nervous system disorders
Stroke
|
1.1%
1/89 • Number of events 1 • Information on adverse events was collected beginning at the time of the intervention and continuing through the end of the study, at 2 weeks post-intervention.
|
|
Cardiac disorders
Myocardial infarction
|
1.1%
1/89 • Number of events 1 • Information on adverse events was collected beginning at the time of the intervention and continuing through the end of the study, at 2 weeks post-intervention.
|
Other adverse events
Adverse event data not reported
Additional Information
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place