Recruitment

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