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A Study to Examine the Effectiveness of Perioperative Rehabilitation and Nutritional Therapy During Gastrectomy

A Phase II Clinical Trial to Examine the Effectiveness of Perioperative Exercise and Nutritional Therapy in Preventing Skeletal Muscle Mass Loss During Gastrectomy - PERIHA study

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000054719
Enrollment
74
Registered
2024-06-20
Start date
2024-06-14
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

gastric cancer

Interventions

In this study, in addition to standard surgical treatment for gastric cancer, perioperative care, and postoperative follow-up, we will implement nutritional therapy (intake of nutritional supplements)
s preferences. Exercise Therapy TheraBand will be provided for patients to perform self-directed training at home. A physical therapist will instruct patients on the training menu as shown in the

Sponsors

Teine Keijinkai Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients with histologically or cytologically confirmed gastric cancer 2. Patients aged 20 years or older at the time of obtaining consent 3. Patients with a disease stage that is expected to be curable by surgery 4. Patients who are either 75 years or older, or have a skeletal muscle index (SMI) of less than 7.8 kg/m2 for males and less than 6.1 kg/m2 for females 5. Patients who have provided written consent of their own free will after fully understanding the details of this study

Exclusion criteria

Exclusion criteria: 1. Patients with concurrent active malignant diseases 2. Patients who cannot undergo body composition analysis using Inbody due to internal metal implants 3. Patients who are unable to take oral intake due to the condition of their gastric cancer 4. Patients deemed inappropriate for participation in this study by the attending physician

Design outcomes

Primary

MeasureTime frame
The skeletal mass index at 6 months post-surgery

Secondary

MeasureTime frame
Analysis of body composition, QOL evaluation using SF-8, and nutritional status assessment using blood tests during the intervention period up to one year post-surgery

Countries

Japan

Contacts

Public ContactKazufumi Umemoto

Teine Keijinkai hospital Department of Surgery

plumk6@gmail.com011-681-8555

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026