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Exercise and Coaching to Slow Aging in Older Blood Cancer Survivors

Tests exercise and behavioral coaching in older survivors of blood cancers.

Plain-language title generated from the registry record
Registry title: Halt Aging in Survivors of Blood Cancers

Key facts

Where
Omaha, United StatesSee the site

Where in United States

  • University of Nebraska Medical CenterOmaha, United StatesTaking people

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Trial details

Who runs it
University of Nebraska
Trial code
NCT07292272
Record updated
1 July 2026
Original description
Older survivors of blood cancer are at a high risk of accelerated biological aging, which increases their risk of developing multiple aging-related conditions. Whereas physical exercise can improve overall health, older cancer survivors do not meet the recommended physical activity, highlighting the need to develop behavioral interventions to increase adherence. Several other knowledge gaps exist to implement exercise interventions in older survivors of blood cancer; the dose and duration of exercise necessary to slow biological aging in older blood cancer survivors remain unknown. To bridge these gaps in knowledge, we have designed a Phase 2 randomized control trial to test the effects of behavioral and exercise interventions on various outcomes.Read full original descriptionShow less

Halt Aging in Survivors of Blood Cancers: the HALTAging-1 Study

Older survivors of blood cancer are at a high risk of accelerated biological aging, which increases their risk of developing multiple aging-related conditions. Whereas physical exercise can improve overall health, older cancer survivors do not meet the recommended physical activity, highlighting the need to develop behavioral interventions to increase adherence. Several other knowledge gaps exist to implement exercise interventions in older survivors of blood cancer; the dose and duration of exercise necessary to slow biological aging in older blood cancer survivors remain unknown. To bridge these gaps in knowledge, we have designed a Phase 2 randomized control trial to test the effects of behavioral and exercise interventions on various outcomes.

Inclusion: Age ≥50 years; A history of hematological malignancy; Participants must be able to and willingly give informed consent.

Exclusion: Patients receiving intensive induction or consolidation chemotherapy. Maintenance chemotherapy, or lower-intensity chemotherapy for an indolent hematological malignancy is allowed; 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; Illnesses such as clinical evidence of decompensated heart failure, unstable angina, or orthopedic or neuromuscular disorders that could limit safe participation in aerobic exercise; Cardiopulmonary exercise test results that preclude safe exercise (e.g., life-threatening arrhythmia, balance difficulties, peak VO2 <10 ml/kg/min); Estimated life expectancy of less than 6 months (that precludes assessment of study primary endpoint); Self-reported pregnancy or the possibility of pregnancy; Participants who do not plan to follow up at the participating center.

ClinicalTrials.gov NCT07292272