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Eine Studie entspricht den Filterkriterien
Kartenansicht
Remote Resistance Exercise Powering Survivors - Gastrointestinal Oncology
Die Details der klinischen Studie sind hauptsächlich auf Englisch verfügbar. Trial Radar KI kann jedoch helfen! Klicken Sie einfach auf 'Studie erklären', um die Informationen zur Studie in der ausgewählten Sprache anzuzeigen und zu besprechen.
Die klinische Studie NCT05664178 untersucht Supportivtherapie im Zusammenhang mit Gastrointestinaler Krebs. Diese interventionsstudie der Phase 1 Phase 2 hat den Status offene rekrutierung und startete am 20. Februar 2023. Es ist geplant, 100 Teilnehmer aufzunehmen. Durchgeführt von H. Lee Moffitt Cancer Center and Research Institute wird der Abschluss für 22. August 2026 erwartet. Die Daten von ClinicalTrials.gov wurden zuletzt am 22. September 2025 aktualisiert.
Kurzbeschreibung
The purpose of the study is to evaluate a tele-resistance training exercise program for individuals undergoing chemotherapy for advanced upper gastrointestinal cancer.
Offizieller Titel
Remote Resistance Exercise Powering Survivors - Gastrointestinal Oncology (Remote REPS - GI)
Erkrankungen
Gastrointestinaler KrebsWeitere Studien-IDs
NCT-Nummer
Studienbeginn (tatsächlich)
2023-02-20
Zuletzt aktualisiert
2025-09-22
Studienende (vorauss.)
2026-08-22
Geplante Rekrutierung
100
Studientyp
Interventionsstudie
PHASE
Phase 1
Phase 2
Phase 2
Status
Offene Rekrutierung
Stichwörter
Gastrointestinal Cancer
Remote Resistance Exercise
GI Cancer Stage III
GI Cancer Stage IV
Tele-Resistance Training
Remote Resistance Exercise
GI Cancer Stage III
GI Cancer Stage IV
Tele-Resistance Training
Primäres Ziel
Supportivtherapie
Zuteilungsmethode
Randomisiert
Interventionsmodell
Parallel
Verblindung
Keine (offene Studie)
Studienarme/Interventionen
| Teilnehmergruppe/Studienarm | Intervention/Behandlung |
|---|---|
ExperimentellTele-Resistance Training (RT) 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. | Tele-resistance Training 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. |
Keine InterventionUsual Care (UC) 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. | Nicht zutreffend |
Hauptergebnismessungen
| Ergebnismessung | Beschreibung der Messung | Zeitrahmen |
|---|---|---|
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 |
Eignungskriterien
Zugelassene Altersgruppen
Erwachsene, Ältere Erwachsene
Mindestalter
18 Years
Zugelassene Geschlechter
Alle
- 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
- 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
H. Lee Moffitt Cancer Center and Research InstituteNationales Krebsinstitut, USA3028 aktive klinische Studien zum ErkundenZentrale Studienkontakte
Kontakt: Nathan Parker, PhD, MPH, 813-745-0527, [email protected]
1 Studienstandorte in 1 Ländern
Florida
Moffitt Cancer Center, Tampa, Florida, 33612, United States
Nathan Parker, PhD, MPH, Kontakt, 813-745-0527, [email protected]
Nathan Parker, PhD, MPH, Hauptprüfer
Martine Extermann, MD, PhD, Prüfarzt
Rutika Mehta, MD, MPH, Prüfarzt
Pamela Hodul, MD, Prüfarzt
Jose Pimiento, MD, Prüfarzt
Richard Kim, MD, Prüfarzt
Dae Won Kim, MD, Prüfarzt
Mohammed Al-Jumayli, MD, Prüfarzt
Daniel Anaya Saenz, MD, Prüfarzt
Jason Denbo, MD, Prüfarzt
Sean Dineen, MD, Prüfarzt
Andrew Sinnamon, MD, Prüfarzt
Jason Fleming, MD, Prüfarzt
Offene Rekrutierung