Ex Onc SLED: a Study Utilizing a Weighted Sled for Horizontal Resistance Training

ConditionCancer
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age20-89
SponsorAllegheny Singer Research Institute (also known as Allegheny Health Network Research Institute)

About this trial

This protocol seeks to analyze patient adherence and outcomes after monitored exercise sessions utilizing primarily weighted sled pushes and pulls for linearly progressed resistance training of individuals who have been diagnosed with cancer.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age 20-89 years

Women of child-bearing potential must verbally confirm lack of pregnancy prior to enrollment. They should also consent to use adequate contraception during the course of the study.

Participants must be determined capable of engaging in resistance training by exercise personnel and/or study PI and must be able to stand.

Participants must complete an assessment by EOC staff and be determined safe to engage in the workout regimen by the study exercise personnel. Any individuals not deemed safe to participate in the basic EOC exercise program will be referred to physical therapy or elsewhere

Disqualifiers

Severe arthritic, joint, cardiovascular, or musculoskeletal condition that would interfere with exercise program

Individuals deemed able to engage in more intense resistance training utilizing compound movements will not be eligible

Pregnant women

Trial population

Individuals diagnosed with cancer on an exercise program at the AHN Exercise Oncology and Resiliency Center

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Change in Adipose Tissue (InBody, kg)

Change in adipose tissue (kg) pre and post resistance training regimen measured via InBody 970 bioelectrical impedance analysis

Time frame
Baseline and study completion, up to 6 months.
2

Change in Adipose Tissue (Ultrasound, Lbs)

Change in adipose tissue (pounds) pre and post resistance training regimen measured via ultrasound.

Time frame
Baseline and study completion, up to 6 months.
3

Change in Muscle Mass

Changes in percent muscle mass (measured by InBody bioelectrical impedance analysis) and percent fat-free mass (measured by ultrasound) from baseline to six months

Time frame
Baseline and study completion, up to 6 months.

Secondary outcomes

1

Intervention Compliance Rate during Exercise Program (Adherence)

Percentage of exercise sessions attended by each participant

Time frame
Through study completion, up to 6 months.
2

Feasibility of the Exercise Program

Tracking of participant completion status.

Time frame
Through study completion, up to 6 months.
3

Adverse Events (Safety)

Time frame
Through study completion, up to 6 months.
4

Changes in Timed Up and Go Test Performance at baseline and post-exercise assessment

An individual stands from a chair, walks ten feet and back, and then sits down. This is timed and recorded in seconds.

Time frame
Baseline and study completion, up to 6 months.

Other outcomes

Sponsors and contacts

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