- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT02120885
An Effect of an Individualized Physical Activity Intervention for Gastric Cancer Patient Undergoing Minimally Invasive Gastrectomy: a Phase III, Prospective Randomized Controlled Trial (Gastric cancer)
Studieoversikt
Status
Forhold
Intervensjon / Behandling
Detaljert beskrivelse
There are many reports on the effect of the exercise program after cancer surgery. In addition, exercise program was associated with improving the QOL and functional recovery, decreasing a mood of depression, maintaining a muscle mass and improving the survival rate.
However, the subject patients of previous studies were Western people. Therefore, The results were not disclosed whether the exercise program suited to the body characteristics of Korean people. Furthermore there was no exercise program studies for the gastric cancer patients.
Medical service for cancer patients care should include not only diagnosis, treatment as like surgery but efforts on enhancing the quality of life. In other words, post-management education and management program as like exercise program are necessary for the cancer patients after surgery. Thus, the investigators have done the pilot study about how to practice the exercise program and how to evaluate the effect on the recovery. Based on the result of pilot study which could identify the safety and the feasibility , the investigators would like to do a prospective randomized controlled study to prove the effect of exercise program after surgery
Studietype
Registrering (Faktiske)
Fase
- Fase 3
Kontakter og plasseringer
Studiesteder
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Seoul, Korea, Republikken, 134
- Yonsei University College of Medicine, Seodaemun-gu, Shinchondong
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Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Beskrivelse
Inclusion Criteria:
- Early gastric cancer patients
- Undergoing minimally invasive surgery
- AGE: 20-70
- ECOG: 0-1
- A patient who did not exercise regularly for the last 6 months
- A patient who signed the informed consent
Exclusion Criteria:
- Pregnancy or plans to become pregnant
- Cognitive disabilities
- Other primary cancer history
- History of major abdominal surgery except current surgery
- Cardiopulmonary medical comorbidity
- Living > 60 km from the hospital
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Støttende omsorg
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Enkelt
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
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Ingen inngripen: Kontrollgruppe
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Eksperimentell: Exercise group
physical activity intervention
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Exercise program is scheduled to be conducted in three phases.
Phase I is in-hospital exercise program.
This program will be conducted in hospital during 1 week after surgery.
Phase II is home-exercise program that will be performed at home during 1 week after discharge.
Phase III is main-exercise program that will be conducted the fitness center nearby hospital during 8 weeks after phase II program.
Main-exercise program is focused on the functional recovery.
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Hva måler studien?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
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QoL(quality of life)
Tidsramme: 10 weeks after gastrectomy
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10 weeks after gastrectomy
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Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
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cardiopulmonary function test
Tidsramme: 10 weeks after gastrectomy
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10 weeks after gastrectomy
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vital signs reflecting of inflammation level
Tidsramme: 10 weeks after gastrectomy
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10 weeks after gastrectomy
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nutrition condition
Tidsramme: 10 weeks after gastrectomy
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10 weeks after gastrectomy
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Samarbeidspartnere og etterforskere
Sponsor
Studierekorddatoer
Studer hoveddatoer
Studiestart (Faktiske)
Primær fullføring (Faktiske)
Studiet fullført (Faktiske)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Anslag)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- 4-2013-0215
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