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Combined Aerobic and Resistance Exercise Training in Metastatic Renal Cell Carcinoma

A Pilot Study of Combined Aerobic and Resistance Exercise Training in Metastatic Renal Cell Carcinoma

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05103722
Enrollment
2
Registered
2021-11-02
Start date
2022-02-17
Completion date
2024-04-01
Last updated
2024-04-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Renal Cell Carcinoma Metastatic

Brief summary

The trial studies the effects of personalized home-based aerobic and resistance exercises on quality of life, changes in physical activity levels, and the change in inflammatory myokines with the exercise intervention in Interleukin 6 (IL-6), C-reactive Protein (CRP), Leptin, Transforming growth factor beta (TGF-beta), and Interferon (INF) gamma.

Interventions

OTHERCombined Aerobic and Resistance Exercise Training

Participants receive personalized exercise plan for home-based two days of aerobic exercises (20-30-minutes) and two days of resistance exercises per week for 12 weeks. After completion of study intervention, participants will be assessed at the of study visit at Week 24.

Sponsors

Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 99 Years
Healthy volunteers
No

Inclusion criteria

* Histologically confirmed diagnosis of RCC * Patients being treated with standard of Programmed cell death protein 1 (anti-PD-1) or anti-PD-L1 immune-checkpoint inhibitor-containing standard of care regimen including patients who are about to start treatment or have been on treatment for a maximum of 4 weeks prior to signing consent * Metastatic Measurable disease, as defined by RECIST 1.1 * Eastern Cooperative Oncology Group (ECOG) performance status of 0-2 with a life expectancy ≥ six months * Physically able to enroll in the exercise program as determined by the treating medical oncologist and after review by Physical medicine and rehabilitation physicians at Johns Hopkins * Adequate bone marrow reserve and organ function measured within 28 days prior to administration of study treatment with the following key parameters: * Hematological: * Absolute neutrophil count ≥ 1.5 × 109/L * Platelets ≥ 100 × 109/L * Hemoglobin≥ 9.0 g/dL * Renal: * Serum Creatinine ≤ 1.5 x the upper limit of normal (ULN) or Calculated Creatinine clearance ≥ 30mL/min * Hepatic: * Total bilirubin ≤ 1.5 x ULN (Patients with known Gilbert disease who have serum bilirubin level ≤ 3 x ULN may be enrolled) * Serum Aspartate aminotransferase (AST) and serum Alanine aminotransferase (ALT) ≤ 2.5 x ULN (For patients with documented liver metastases AST and/or ALT ≤ 5 x ULN)

Exclusion criteria

* The presence of bone metastasis in the spine, pelvis, and lower limbs * Currently physically active or moderately active as determined by Leisure Score Index of Godin Leisure-Time Exercise Questionnaire (GSLTPAQ) * History of underlying cardiovascular, respiratory, musculoskeletal disease or joint problems that preclude moderate physical activity * Known underlying uncontrolled brain metastatic lesions requires steroids therapy and/or radiotherapy * Major surgery within four weeks prior to enrollment. * Radiotherapy for RCC 28 days prior to week 1 day 1

Design outcomes

Primary

MeasureTime frame
Number of participants who adhere to the exercise intervention2 years

Secondary

MeasureTime frameDescription
Percentage of patients screened compared to patients enrolled2 years
Percentage of patients who remained in the study and didn't drop off the study after enrollment2 years
Change in HRQoL as measured by FACT-G QuestionnaireBaseline, Week 4, Week 8, Week 12 and Week 24There are 27 items in Functional Assessment of Cancer Therapy: General (FACT-G) questionnaire, and they are scored on a scale from 0 to 4; 0 being Not at All, and 4 being Very much.
The incidence of grade 3-5 toxicities as per CTCAE 5.02 years

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026