Remote Resistance Exercise Powering Survivors - Gastrointestinal Oncology

NCT05664178 | Recruiting Phase 1

• 2 other identifiers: MCC-217421K22CA262352-01
• Study Type: interventional
• Target: 100
• Locations: 1 country
• Sites: 1

Brief Summary

The purpose of the study is to evaluate a tele-resistance training exercise program for individuals undergoing chemotherapy for advanced upper gastrointestinal cancer.

Conditions

Gastrointestinal Cancer

Keywords

Gastrointestinal Cancer; Remote Resistance Exercise; GI Cancer Stage III; GI Cancer Stage IV; Tele-Resistance Training

Outcome Measures

Primary Outcomes (22)

• Percentage of Participants that Enroll and Consent - Enrollment Feasibility

  Enrollment will be considered feasible if ≥ 70% of eligible and approached patients actually consent and enroll

  Up to 36 Months

• Percentage of Participants that Complete Study Assessments - Retention Feasibility

  Retention will be considered feasible if ≥ 70% of participants who complete baseline measures also complete followup measures

  Up to 3 Months

• Exercise Adherence - Feasibility

  Exercise adherence will be assessed based on performance of prescribed exercise volume, with tele-RT volumes considered feasible if participants perform ≥ 70% of the volume prescribed.

  Up to 6 Months

• Participant Evaluation of Feasibility and Acceptability - Acceptability

  Participants evaluation of feasibility and acceptability will be assessed with a questionnaire, adapted to fit the intervention. The questionnaire includes both Likert Scale and open-ended questions. An item-by-item basis and as average item score, with scores ≥4 ("agree" to "strongly agree") indicating acceptability. Open-ended responses will be analyzed qualitatively to inform intervention improvement.

  Up to 6 Months

• Participant Self-Reported Musculoskeletal Injuries - Safety

  Participants will be asked to report the following information: type (joint or soft tissue or other), location (specific body part), and cause (description of activity during which injury was incurred). Participants will then rate the injury on a scale of 1-4 (1=not related, 2=unlikely related, 3=likely related, 4=definitely related). The severity of the injury will be rated on a scale of 1-4 (1=mild/no change in daily activity, 2=some limitation of daily activity, 3=major limitation of daily activity, 4=life threatening). The duration for which daily activities were impacted will be rated on a scale from 1-5 (1=no change, 2=1-3 days, 3=4-7 days, 4=1-2 weeks, 5=more than 2 weeks). The numerator of the variable used to determine program safety will be the number of musculoskeletal injuries that were rated at least a 3 for relatedness to RT (likely related or definitely related) and caused at least some limitation of daily activity lasting more than 3 days.

  Up to 6 Months

• Participant Muscular Strength - Baseline

  Muscular strength will be measured using four separate 1-repetition maximum (1RM) lifts: chest press, seated row, leg press, and leg extension performed on resistance training machines. If a particular 1RM lift is contraindicated for a given participant (e.g., limited range of motion for a given joint or osteoporosis), the lift will be skipped, or 5-repetition maximum (5RM) will be measured instead of 1RM, and 1RM will be estimated from 5RM.

  At Baseline

• Participant Muscular Strength - Follow-up

  Muscular strength will be measured using four separate 1-repetition maximum (1RM) lifts: chest press, seated row, leg press, and leg extension performed on resistance training machines. If a particular 1RM lift is contraindicated for a given participant (e.g., limited range of motion for a given joint or osteoporosis), the lift will be skipped, or 5-repetition maximum (5RM) will be measured instead of 1RM, and 1RM will be estimated from 5RM.

  Up to 6 Months

• Participant Muscular Endurance - Baseline

  Muscular endurance will be measured by the maximum number of repetitions a participant can perform at 70% of the baseline 1-repetition maximum (1RM) for the same four lifts

  At Baseline

• Participant Muscular Endurance - Follow-up

  Muscular endurance will be measured by the maximum number of repetitions a participant can perform at 70% of the baseline 1-repetition maximum (1RM) for the same four lifts

  Up to 6 Months

• Participant Skeletal Muscle Index (SMI) - Baseline

  Participants SMI will be measured using Tomovision SliceOMatic software and clinical, computerized tomography (CT) scans from baseline to follow up.

  At Baseline

• Participant Skeletal Muscle Index (SMI) - Follow-up

  Participants SMI will be measured using Tomovision SliceOMatic software and clinical, computerized tomography (CT) scans from baseline to follow up.

  Up to 6 Months

• Participant Skeletal Muscle Density (SMD) - Baseline

  Participants SMD will be measured using Tomovision SliceOMatic software and clinical, computerized tomography (CT) scans from baseline to follow up.

  At Baseline

• Participant Skeletal Muscle Density (SMD) - Follow-up

  Participants SMD will be measured using Tomovision SliceOMatic software and clinical, computerized tomography (CT) scans from baseline to follow up.

  Up to 6 Months

• Participants Health-Related Quality of Life

  Health-related quality of life will be measured using the Functional Assessment of Cancer Therapy-General (FACT-G)

  Up to 6 Months

• Participant Fatigue

  Participant fatigue will be measured using the FACT-Fatigue questionnaire (FACT-F)

  Up to 6 Months

• Participant Physical Functioning

  Participants physical functioning will be measured using the Patient Reported Outcomes Measurement Information System (PROMIS) Physical Functioning Short Form

  Up to 6 Months

• Participant Chemotherapy-induced peripheral neuropathy (CIPN)

  Participant CIPN will be measured using the European Organization of Research and Treatment of Cancer (EORTC) Quality of Life Questionnaire-CIPN twenty-item scale (QLQ-CIPN20)

  Up to 6 Months

• Participant Self Reported Exercise - Baseline

  Participant self-reported exercise will be measured using a modified Godin Leisure Time Exercise Questionnaire to assess both aerobic and resistance exercise

  At Baseline

• Participant Self Reported Exercise - Follow-up

  Participant self-reported exercise will be measured using a modified Godin Leisure Time Exercise Questionnaire to assess both aerobic and resistance exercise

  Up to 6 Months

• Participant Clinicodemographic Characteristics - Baseline

  Participant clinicodemographic characteristics including tumor type and cancer stage, chemotherapy type, sex, age, body mass index, race/ethnicity, and marital status will be collected from participants' electronic medical records.

  At Baseline

• Participant Clinicodemographic Characteristics - Follow-up

  Participant clinicodemographic characteristics including tumor type and cancer stage, chemotherapy type, sex, age, body mass index, race/ethnicity, and marital status will be collected from participants' electronic medical records.

  Up to 6 Months

• Participant Treatment Outcome

  Participant relevant treatment outcomes including chemotherapy dose reductions and changes in chemotherapy will be collected from participants' electronic medical records.

  Up to 6 Months

Study Arms (2)

Tele-Resistance Training (RT)

EXPERIMENTAL

Participants will be encouraged to perform approximately 30 minutes of resistance training exercises approximately twice per week for 12 weeks. Participants will also be encouraged to perform moderate aerobic exercise at least 3 times per week. Participants will wear a FitBit fitness watch to monitor aerobic exercise.

Behavioral: Tele-Resistance Training

Usual Care (UC)

NO INTERVENTION

Participants randomized to the Usual Care (UC) arm will be provided with information materials outlining resistance training using body weight or basic equipment. Participants will wear a FitBit fitness watch to monitor aerobic exercise.

Interventions

Tele-Resistance Training BEHAVIORAL

Tele-Resistance training sessions will be supervised and guided by a certified exercise trainer via smartphone, tablet or laptop. Exercises will be performed using resistance tubes (Bodylastics Resistance Bands Set) and a connectable bar (Bionic Body Workout Bar) that mimics a weighted barbell when tubes are attached. The tubes provide up to 142 pounds of resistance (adjustable in increments between 3-10 pounds) when simultaneously connected to handles or bar, and multiple tubes can be attached simultaneously. Participants will engage in brief warm up exercises lasting 2-3 minutes prior to each RT session and will rest at least 1 minute between sets of the same exercise to aid muscle recovery. Participants will perform at least 2 sets of 12 repetitions for each of 6 exercises. Including warm up, training sets, and rest, sessions will last approximately 30 minutes. RT will include six target exercises focusing on major muscle groups of the upper body, lower body, and core.

Tele-Resistance Training (RT)

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Age ≥ 18 years
• Biopsy-proven upper GI cancer, stage III-IV
• ECOG performance status 0-1
• Treatment plan of chemotherapy with planned return to Moffitt Cancer Center for restaging
• Able to read and speak English fluently
• Capable of providing informed consent

You may not qualify if:

• Regular engagement in RT (2x/week targeting all major muscle groups)
• Screen failure for exercise safety based on Physical Activity Readiness Questionnaire (PAR-Q) and Patient-Reported Measurement Information System (PROMIS) screening questions
• Underlying unstable cardiac or pulmonary disease or symptomatic cardiac disease (New York Heart Association functional class III or IV).
• Recent fracture or acute musculoskeletal injury that precludes ability to participate in RT
• Numeric pain rating scale of ≥ 7 out of 10
• Myopathic or rheumatologic disease that impacts physical function

Sponsors & Collaborators

• H. Lee Moffitt Cancer Center and Research Institute: lead
• National Cancer Institute (NCI): collaborator

Study Sites (1)

Moffitt Cancer Center

Tampa, Florida, 33612, United States

RECRUITING

Related Links

• Moffitt Cancer Center Clinical Trials Search

MeSH Terms

Conditions

Gastrointestinal Neoplasms

Condition Hierarchy (Ancestors)

Digestive System Neoplasms; Neoplasms by Site; Neoplasms; Digestive System Diseases; Gastrointestinal Diseases

Study Officials

• Nathan Parker, PhD, MPH

  Moffitt Cancer Center

  PRINCIPAL INVESTIGATOR

Central Study Contacts

Nathan Parker, PhD, MPH

CONTACT

813-745-0527; Nathan.Parker@moffitt.org

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: SUPPORTIVE CARE
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: December 9, 2022
• First Posted: December 23, 2022
• Study Start: February 20, 2023
• Primary Completion (Estimated): August 22, 2026
• Study Completion (Estimated): August 22, 2026
• Last Updated: February 27, 2026

Record last verified: 2026-02

Locations

US (1)