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NCT06989463 · ClinicalTrials.gov registry record · NA
Complementary Behavioral Interventions To Remediate Cognitive Impairment or Emotional Distress in Cancer Survivors
A NA study of Survivors of Childhood Cancer, sponsored by St. Jude Children's Research Hospital.
- Active
- Registry status
- NA
- Development phase
- 20
- Enrollment target
- 1
- Study location
NCT06989463 is a NA study of Survivors of Childhood Cancer that is active but no longer recruiting, run by St. Jude Children's Research Hospital. The registered enrollment target is 20 participants, below the 70-participant average among 3 other Survivors of Childhood Cancer trials with a reported enrollment target (71% lower). The trial reports 1 study location across 1 state.
The verdict
NCT06989463, a NA study of Survivors of Childhood Cancer, is active but no longer recruiting, sponsored by St. Jude Children's Research Hospital.
- ACTIVE NOT RECRUITING
- Registry status
- NA
- Development phase
- 20 participants
- Enrollment target
- 1
- Study location
Study Summary
Childhood cancer survivors are at risk for accelerated aging due to the specific treatments they have received to cure their cancer. Several interventions, including exercise, cognitive training, and mindfulness practice, have been developed and studied for effectiveness among participants in the St. Jude Lifetime Cohort (SJLIFE) to mitigate these effects. The interventions offered thus far have not included two components at the same time. The purpose of this study is to determine whether or not adult cancer survivors enrolled in SJLIFE will participate in two interventions at the same time. The combined interventions will include exercise plus cognitive training or exercise plus mindfulness practice. Each intervention will be conducted over a 12-week period. Participants will also be asked to complete follow-up testing after the 12-week intervention period is completed. Primary Objectives • To determine the acceptability of a two-component intervention (exercise (EX) plus cognitive training (CT) or exercise (EX) plus mindfulness practice (MP)) among survivors of childhood cancer with either cognitive impairment or emotional distress. Hypotheses: * 45% of those approached for participation in each arm of this study will enroll on the study. * Among those who enroll, 70% will complete the follow-up testing at 12 weeks. * Among those who completed the follow-up testing, the mean attendance to the intervention sessions will be 70% on each of their two interventions. That is, they will complete 70% of exercise sessions and 70% of either cognitive training or mindfulness practice. * To identify barriers and facilitators to intervention adherence. Hypotheses: * Participants will identify features of the study processes that either facilitate or discourage adherence. * Participants will identify features of the intervention technology and intervention components that either facilitate or discourage adherence. * Participants will identify personal factors that facil
Conditions Studied
Interventions
- OTHER 12 Week Exercise Intervention
- OTHER Cognitive Training Intervention
- OTHER Mindfulness practice intervention
Study Locations (1)
Tennessee
- St. Jude Children's Research Hospital - Memphis
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 20 participants |
| Start Date | 2025-07-29 |
| Est. Completion | 2026-11 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06989463
The ClinicalTrials.gov registry entry for NCT06989463 describes a study currently listed as active not recruiting, categorized as NA. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 70-participant average among 3 other Survivors of Childhood Cancer trials with a reported enrollment target (71% lower). The listed sponsor is St. Jude Children's Research Hospital, which has 410 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Survivors of Childhood Cancer appearing as the primary indexed condition, and to 3 interventions - of which 12 Week Exercise Intervention is the first listed.
NCT06989463 reports 1 study location spanning 1 distinct geographic area - top geographies include Tennessee.
Frequently Asked Questions
What is clinical trial NCT06989463 about?
NCT06989463 is a clinical study titled "Complementary Behavioral Interventions To Remediate Cognitive Impairment or Emotional Distress in Cancer Survivors". Childhood cancer survivors are at risk for accelerated aging due to the specific treatments they have received to cure their cancer. Several interventions, including exercise, cognitive training, and mindfulness practice, have been developed and studied for effectiveness among participants in the St...
What is the current status of trial NCT06989463?
This trial is currently active not recruiting. It is a NA study. The enrollment target is 20 participants. The study started on 2025-07-29. Estimated completion is 2026-11.
What conditions does trial NCT06989463 study?
This clinical trial studies the following conditions: Survivors of Childhood Cancer.
What interventions are being tested in trial NCT06989463?
The interventions under investigation include: 12 Week Exercise Intervention (OTHER), Cognitive Training Intervention (OTHER), Mindfulness practice intervention (OTHER).
Who is sponsoring clinical trial NCT06989463?
This trial is sponsored by St. Jude Children's Research Hospital, which has 410 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06989463 being conducted?
This trial has 1 study location across Tennessee. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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