Halt Aging in Survivors of Blood Cancers: the HALTAging-1 Study
NCT ID: NCT07292272
Last Updated: 2025-12-26
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
PHASE2
180 participants
INTERVENTIONAL
2026-02-01
2032-02-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
OTHER
NONE
Study Groups
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Intervention Arm-Supervised
intervention arm incorporating virtually supervised moderate-intensity aerobic exercise and behavioral intervention/coaching to improve adherence
Supervised Exercise and Coaching
Intervention arm incorporating virtually supervised moderate-intensity aerobic exercise and behavioral intervention/coaching to improve adherence
Enhanced Usual Care-Virtual Gym
enhanced usual care arm, where survivors will get access to virtual gym membership only.
Virtual Gym Membership
This arm will get access to a virtual gym membership only
Interventions
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Supervised Exercise and Coaching
Intervention arm incorporating virtually supervised moderate-intensity aerobic exercise and behavioral intervention/coaching to improve adherence
Virtual Gym Membership
This arm will get access to a virtual gym membership only
Eligibility Criteria
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Inclusion Criteria
2. A history of hematological malignancy
3. Participants must be able to and willingly give informed consent
Exclusion Criteria
2. Neurodegenerative disease (e.g. Alzheimer's dementia), stroke, or uncontrolled psychotic disorders (e.g. schizophrenia or bipolar disorder) in the past 3 months if those disorders are considered significant enough to impair participation in the study.
3. Illnesses such as clinical evidence of decompensated heart failure, unstable angina, or orthopedic or neuromuscular disorders that could limit safe participation in aerobic exercise.
4. Cardiopulmonary exercise test results that preclude safe exercise (e.g., life-threatening arrhythmia, balance difficulties, peak VO2 \<10 ml/kg/min).
5. Estimated life expectancy of less than 6 months (that precludes assessment of study primary endpoint).
6. Participants who do not plan to follow up at the participating center.
50 Years
ALL
No
Sponsors
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University of Nebraska
OTHER
Responsible Party
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Locations
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University of Nebraska Medical Center
Omaha, Nebraska, United States
Countries
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Central Contacts
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Facility Contacts
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IIT Office IIT Office
Role: primary
Other Identifiers
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606-25-FB
Identifier Type: -
Identifier Source: org_study_id