Progressive Resistance Training for the Improvement of Physical Function

OHSU Knight Cancer Institute

Status

Completed

Conditions

Sarcoma

Treatments

Other: Quality-of-Life Assessment

Other: Exercise Counseling

Other: Questionnaire Administration

Other: Resistance Training

Study type

Interventional

Funder types

Other

NIH

Identifiers

NCT04247425

SOL-19103-L (Other Identifier)

P30CA069533 (U.S. NIH Grant/Contract)

NCI-2019-05865 (Registry Identifier)

STUDY00019942 (Other Identifier)

Details and patient eligibility

About

This trial studies how well progressive resistance training works in improving the physical function of sarcoma survivors. Treatments for sarcoma can cause side effects such as fatigue, muscle loss, and weakness, which can negatively impact a patient's ability to physically function and enjoy an independent lifestyle. Engaging in a resistance training exercise routine may improve physical function, body composition, and bone density of sarcoma survivors.

Full 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 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.

Enrollment

10 patients

Sex

All

Ages

15+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Eligible for the Sarcoma Survivorship Registry (Institutional Review Board [IRB] #12039)
- History of histologically-confirmed sarcoma
- History of treatment with surgery, radiation and/or chemotherapy for the sarcoma diagnosis
- Completion of sarcoma treatment >= 2 years prior to study enrollment
- No evidence of recurrent or residual disease on surveillance exam or imaging for at least 2 years prior to study enrollment
Sarcoma location must have been in the extremities, body wall, pelvic/shoulder girdle or axial skeleton. Intra-thoracic, intra-abdominal or cranial sarcomas are not eligible
Currently engaging in < 1 hour of resistance exercise per week by self-report. Examples of resistance exercise include: using free weights or weight machines, push-ups, sit-ups, lunges, plank, etc.
Able and willing to commit to attending weekly video coaching sessions and independently completing weekly resistance training sessions. This requires access to internet and a device with video and audio capabilities. A webcam may be provided by the study to the participant if needed
Able and willing to commit to attending one initial in-person training session and one in-person follow-up assessment
Ability to understand and willingness to sign a written informed consent document

Exclusion criteria

Medical contraindication(s) to any and all resistance training as determined by treating physician
Non-English speaking. At this time, we do not have resources to support translation of exercise physiologist (EP) sessions
Dependent on a mobility device (e.g., crutches, wheelchair) for independent activities of daily living (IADLs)
- Use of a cane is permitted
Participant has known psychiatric or substance abuse disorders that would interfere with cooperation with the requirements of the trial
Any condition that, in the opinion of the investigator, would interfere with evaluation of study treatment or interpretation of participant safety or study results (e.g., pregnancy)