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| ID | Type | Description | Link |
|---|---|---|---|
| HUM00218780 | Other Identifier | University of Michigan |
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This pilot study will be a prospective, single arm study to investigate the feasibility and acceptability of a brief, telehealth, cognitive compensatory training intervention for children with a history of pediatric cancer at the University of Michigan. Study aims to enroll 10 children with a history of treatment for pediatric cancer, along with their caregiver.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Intervention | Experimental | The intervention will include 5 weekly sessions (60-90 minutes each) of cognitive compensatory training (CCT) delivered virtually by a pediatric neuropsychologist. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Cognitive Compensatory Training | Other | The intervention will include 5 weekly sessions (60-90 minutes each) of cognitive compensatory training (CCT) delivered virtually by a pediatric neuropsychologist. |
| Measure | Description | Time Frame |
|---|---|---|
| Determining satisfaction and perceived benefit from study intervention based off of change in results from the BRIEF-2 questionnaire from baseline to 6 weeks post trial entry | Completion of Study Questionnaire, BRIEF-2, at time of enrollment at after intervention completion. | 6 weeks from trial entry |
| Determining satisfaction and perceived benefit from study intervention based off of change in results from the Conners 3 questionnaire from baseline to 6 weeks post trial entry | Completion of Study Questionnaire, Conners 3, at time of enrollment at after intervention completion. | 6 weeks from trial entry |
| Determining satisfaction and perceived benefit from study intervention based off of change in results from the SMALSI-2 questionnaire from baseline to 6 weeks post trial entry | Completion of Study Questionnaire, SMALSI-2, at time of enrollment at after intervention completion. | 6 weeks from trial entry |
| Determining satisfaction and perceived benefit from study intervention based off of change in results from the SPSI-R questionnaire from baseline to 6 weeks post trial entry | Completion of Study Questionnaires, SPSI-R , at time of enrollment at after intervention completion. | 6 weeks from trial entry |
| Determining satisfaction and perceived benefit from study intervention based off of change in results from the PKEQ questionnaire from baseline to 6 weeks post trial entry | Completion of Study Questionnaires, PKEQ, at time of enrollment at after intervention completion. | 6 weeks from trial entry |
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| Measure | Description | Time Frame |
|---|---|---|
| Study completion | Possible factors contributing to study completion will be gathered from the History Questionnaire | 6 weeks from trial entry |
| Clinical outcomes based off of response to the BRIEF-2 study questionnaire |
Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Kaitlin McCloskey | University of Michigan Rogel Cancer Center | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of Michigan | Ann Arbor | Michigan | 48109 | United States |
PI does not plan to share IPD
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| ID | Term |
|---|---|
| D009369 | Neoplasms |
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Clinical outcomes of the intervention will also be summarized using empirically validated caregiver and child responses to the BRIEF-2 questionnaire
| 6 weeks from trial entry |
| Clinical outcomes based off of response to the Conners 3 study questionnaire | Clinical outcomes of the intervention will also be summarized using empirically validated caregiver and child responses to the Conners 3 questionnaire | 6 weeks from trial entry |
| Clinical outcomes based off of response to the SMALSI-2 study questionnaire | Clinical outcomes of the intervention will also be summarized using empirically validated caregiver and child responses to the SMALSI-2 questionnaire | 6 weeks from trial entry |
| Clinical outcomes based off of response to the SPSI-R study questionnaire | Clinical outcomes of the intervention will also be summarized using empirically validated caregiver and child responses to the SPSI-R questionnaire | 6 weeks from trial entry |
| Clinical outcomes based off of response to the PKEQ study questionnaire | Clinical outcomes of the intervention will also be summarized using empirically validated caregiver and child responses to the PKEQ questionnaire | 6 weeks from trial entry |