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临床试验/DRKS00033612
DRKS00033612尚未招募Unknown

A multicenter prospective randomized controlled trial to test the safety and efficacy of a systematic app-based remote and home-based prehabilitation program in comparison to education only before major surgeries: The LUMOS Study. - LUMOS

Goethe Universität Frankfurt am Main, Universitätsklinikum Frankfurt0 个研究点目标入组 382 人开始时间: 2024年5月13日最近更新:

试验速览

阶段
Unknown
状态
尚未招募
发起方
入组人数
382

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomized controlled study
盲法
Open (masking not used)

入排标准

年龄范围
18 Years 至 75 Years(—)
性别
All

入选标准

  • Written informed consent
  • - Willing to participate
  • - Patients have an Android or iOS-based smartphone
  • - Patients who are planned for one of the following surgeries as the leading and initial OPS-code are eligible to participate in the LUMOS trial in case of missing contra-indications and exclusions. OPS codes in accordance with the DIMDI OPS version 2024: https://klassifikationen.bfarm.de/ops/kode-suche/htmlops2024/index.htm:
  • 5-070 to 5-073, 5-077 to 5-079 (endocrine glands)
  • 5-314, 5-316, 5-32 to 5.334, 5-339 to 5-349 (trachea, lung and bronchus)
  • 5-38 to 5-39 (vascular surgeries without cardiovascular surgery)
  • 5-404.1 to 5-405, 5-406.2 to 5-406.9+a+b, 5-407 (lymphadenectomies)
  • 5-413 and 5-419 (splenectomy)
  • 5-423 to 5-427 (esophagectomy)
  • 5-434 to 5-438 (gastrectomy)
  • 5-445 and 5-446 (non resecting gastric bypass operations)
  • 5-454 (small bowel resections)
  • 5-455 and 4-466 (large bowel resections including Hartmann’s revision)
  • 5-456 (proctocolectomy)
  • 5-484 and 5-485 (rectum resections)
  • 5-502 and 5-503 (anatomical liver resection)
  • 5-512, 5-515, 5-518.4 and .5, 5-519 (biliary tract resections)
  • 5-523, 5-524, 5-525, 5-527 and 5-529 (pancreas resections and draining procedures)
  • 5-536, 5-538, 5-539 (abdominal wall hernias)
  • 5-553, 5-554, 5-575 to 5-579, 5-604 (urologic resections: kidney, bladder, prostate)
  • 5-652, 5-653, 5-661, 5-682 to 5-687 (gynecologic resections of uterus, ovary, cervix)
  • 5-87 and 5-88 (breast surgery)

排除标准

  • - Younger than 18 years
  • - Currently pregnant or breastfeeding (anamnestically)
  • - Unable to understand the rationale and the aims of the proposed training program
  • - Unable to interact with the application
  • - Patients with an ECOG performance status >3.
  • - Patients unable to walk, run, step, or cycle.
  • - Patients with an acute (on chronic) cardiovascular disease
  • Acute myocardial infarction or unstable angina (acute phase) (I20.0, I21)
  • Uncontrolled arrhythmias causing symptoms or hemodynamic compromise
  • Acute myocarditis or pericarditis (I30, I39, I40)
  • - Suspected dissecting aneurysm
  • - Uncontrolled acutely decompensated HF (acute pulmonary edema) (J81)
  • - HR>120 bpm, BP> 180mmHg sys, 120mmHg diastolic
  • -Patients with an acute (on chronic) pulmonary disease
  • -Acute pulmonary embolism (I26)
  • -Resting dyspnea (Frequency>25)
  • -Exertional dyspnea after less than 2 floors of step walking
  • -Chest pain when resting
  • -Severe hypoxemia at rest or acute respiratory failure (J80)
  • -An acute, non-cardiopulmonary disorder that may affect exercise performance or be aggravated by exercise (such as infection, renal failure, or thyrotoxicosis)
  • -Mental impairment leading to inability to cooperate
  • -Patients under guardianship or imprisoned

研究者

发起方
Goethe Universität Frankfurt am Main, Universitätsklinikum Frankfurt

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