Skip to content

Feasibility study of combined aerobic exercise and strength training during neoadjuvant chemotherapy for resectable adenocarcinoma of the stomach or gastroesophageal junction.

Feasibility study of combined aerobic exercise and strength training during neoadjuvant chemotherapy for resectable adenocarcinoma of the stomach or gastroesophageal junction. - SPIN-Pilot

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00005607
Enrollment
20
Registered
2014-04-10
Start date
2014-06-01
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

locally advanced adenocarcinoma of the stomach or gastroesophageal junction (AEG I-III) C16

Interventions

Group 1: Preoperative combined aerobic exercise and strength training during neoadjuvant Chemotherapy for 10-12 weeks. Training occurs in 2 phases: - supervised exrcise training: twice weekly under su

Sponsors

Klinikum rechts der Isar der TU München
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.) Histologically verified, resectable Adenocarcinoma of the stomach or the esophageal-gastric-junction (AEG I-III), stage uT2 - uT4 without distant metastases. 2.) age = 18 years 3.) 3.) ECOG Status 0-2 4.) negative pregnancy test for women of childbearing-potential 5.) Sufficient bone-marrow, hepatic and renal function by assessment of the treating oncologist

Exclusion criteria

Exclusion criteria: 1.) non-resectable primary tumour by assessment of the treating surgeon. 2.) Participation in an interventional trial with interefering primary endpoint. 3.) pregnancy or breat-feeding 4.) severe cardiac comorbidities (instable angina pectoris, congestive heat failure NYHA IV, malignent arteriell Hypertension). 5.) severe pulmonary comorbidities (COPD GOLD IV) 6.) Muscoloskeletall comorbidities (e.g. coxarthritis, Gonarthritis) that significantly limit mobility 7.) lack of compliance 8.) other reasons that impede physical exercise training

Design outcomes

Primary

MeasureTime frame
Postoperative Morbidity and Mortality according to Dindo-Clavien Grade II-IV

Secondary

MeasureTime frame
1.) number of patients enrolled within the recruiting period 2.) number of screened patients 3.) Number of patients that finish the exercise training (compliance) 4.) drop-out rate

Countries

Germany

Contacts

Public ContactAndre L. Mihaljevic

Klinikum rechts der Isar,Technische Universität München

andre.mihaljevic@tum.de+498941405145

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026