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Application of lifelog-based physical activity and nutritional intervention for minimizing postoperative weight-loss among esophageal cancer patients.

Application of lifelog-based physical activity and nutritional intervention for minimizing postoperative weight-loss among esophageal cancer patients.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0006446
Enrollment
94
Registered
2021-08-13
Start date
2022-08-25
Completion date
Unknown
Last updated
2022-10-24

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

Conditions

None listed

Interventions

Behavioral, Dietary Supplement : In order to prevent weight loss and increase skeletal muscle mass, for the intervention group, exercise and nutritional interventions with optimal life-log will be giv

Sponsors

National Research Foundation
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Those who have been diagnosed with esophageal cancer and are over the age of 18 who are scheduled to undergo curative esophageal resection and reconstruction, and are under 80 years of age – Able to walk independently and live daily life - ECOG PS 0-1 – Those who can use a smartphone – Those who signed on the written informed consent to this study

Exclusion criteria

Exclusion criteria: - Those who have limited cognitive and communication skills or are currently receiving psychiatric treatment – Those who have had esophageal cancer treatment (surgery) within the last 1 year (excluding local treatments such as endoscopic resection) – Those who have previously had esophageal resection and reconstructive surgery – Those who are overseas residents or foreigners, and cannot be continuously followed – Those who are with limited physical ability to perform this intervention program: 1) Cardiac failure (New York Heart Association functional classes III and IV)) due to cardiovascular disease or cerebrovascular disease (cerebral hemorrhage, cerebral infarction, transient ischemic attack, stroke, cerebrovascular accident) If you are concerned about the worsening of the disease. 2) Patients unable to walk due to joint problems or paralysis 3) Patients with kidney dysfunction(estimated GFR<60mL/min/1.73m^2) 4) Patients who failed to proceeding to suffiecient oral intake postoperatively 5) Patients who did not meet the oral intake initiation within 14 days after surgery *Indication for drop-out: Inhospitalization more than 30-day after surgery since postoperative complication

Design outcomes

Primary

MeasureTime frame
Incidence of severe weight loss (= 10% comparing to pre-surgery weight)

Secondary

MeasureTime frame
1) Body weight (kg), body fat percentage (%), skeletal muscle mass index (SMI, kg/m2) measured by Bioelectrical impedance analysis (BIA), abdominal SMI(kg/m2) at lumbar 3 level and abdominal body fat percentage (%) measured by CT ;2) Quality of life and symptoms: EORTC QLQ-C30 & OES18, GSRS, depression (PHQ9) , Distress(NCCN distress thermometer and problem list); 3) Nutritional indicators (Lab): PNI, NRI (e.g. albumin, total protein, Hb, WBC, ANC, ALC, platelet, NLR, PLR); 4) Nutritional evaluation score: NRS-2002, MNA-SF, dietary habit (intake questionnaire, nutrition counseling), amount of oral intake(kcal, protein); 5) Physical function: grip (kg), 6MWT (m), CS (rep), physical activity level (step, MVPA during last 7-day);6) Complications within 2 months after surgery

Countries

Korea, Republic of

Contacts

Public ContactYoung Mog Shim

Samsung Medical Center

genehee.lee@samsung.com+82-2-3410-1062

Outcome results

None listed

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