Progressive Resistance Training for the Improvement of Physical Function
Last updated on July 2021Recruitment
- Recruitment Status
- Active, not recruiting
- Estimated Enrollment
- Same as current
Summary
- Conditions
- Sarcoma
- Type
- Interventional
- Phase
- Not Applicable
- Design
- Allocation: N/AIntervention Model: Single Group AssignmentMasking: None (Open Label)Primary Purpose: Supportive Care
Participation Requirements
- Age
- Between 15 years and 125 years
- Gender
- Both males and females
Description
PRIMARY OBJECTIVE: I. To determine the feasibility of a home-based individualized progressive resistance training (PRT) program in sarcoma survivors. SECONDARY OBJECTIVES: I. To assess secondary measures of feasibility of a home-based, individualized PRT program in sarcoma survivors. II. To determin...
PRIMARY OBJECTIVE: I. To determine the feasibility of a home-based individualized progressive resistance training (PRT) program in sarcoma survivors. SECONDARY OBJECTIVES: I. To assess secondary measures of feasibility of a home-based, individualized PRT program in sarcoma survivors. II. To determine if a 3-month PRT program improves physical function in sarcoma survivors. EXPLORATORY OBJECTIVE: I. To determine if a 3 month resistance training program improves body composition and bone mineral density. OUTLINE: Patients complete a series of progressive resistance training exercises at home twice weekly over 1 hour and receive instructional guidance from an exercise physiologist via videoconferencing once per week during one of these sessions for up to 12 weeks. After completion of study, patients are followed up at 3 months.
Tracking Information
- NCT #
- NCT04247425
- Collaborators
- National Cancer Institute (NCI)
- Oregon Health and Science University
- Investigators
- Principal Investigator: Lara E Davis OHSU Knight Cancer Institute