Меню
Идёт набор NCT07324447

EFFECTS OF SUPERVISED PHYSICAL EXERCISE AFTER BARIATRIC SURGERY ON MUSCLE MASS AND BONE DENSITY (OBEFIT STUDY)

Без фазы С лечением Obesity &Amp;Amp; Overweight Bariatric Surgery Physical Exercise

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: physical exercise programme.
Кому может быть актуально
Состояния в реестре: Obesity &Amp;Amp; Overweight, Bariatric Surgery, Physical Exercise. Базовые параметры: от 18 лет · Все.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
Испания
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

CLINICAL TRIAL ON THE EFFECT OF SUPERVISED PHYSICAL EXERCISE AFTER BARIATRIC SURGERY ON MUSCLE MASS AND BONE DENSITY (OBEFIT STUDY)

Обзор

CLINICAL TRIAL ON THE EFFECT OF SUPERVISED PHYSICAL EXERCISE AFTER BARIATRIC SURGERY ON MUSCLE MASS AND BONE DENSITY (OBEFIT STUDY)

Подробное описание

Introduction Background and rationale Obesity is currently a complex disease that has reached pandemic proportions and affects millions of people worldwide. Bariatric surgery can generate adverse side effects such as loss of bone mineral density, loss of muscle mass, reduction in cardiorespiratory capacity. Therefore, accompanying medical treatment with an individualised physical exercise intervention can generate a multitude of health benefits for the patient.

Objectives

As main objective the investigators focus on:

\- To determine the differences in muscle mass and bone density in patients undergoing bariatric surgery who have undergone a post-operative supervised physical exercise programme and no exercise programme.

* To determine the differences in muscle function using the hand grip test. * To determine BMD loss using densitometry.

Secondary objectives:

* To analyse maximal fat oxidation throughout the whole process from metabolic inflexibility to metabolic flexibility). * To determine differences in body composition. * To determine the resolution of type 2 diabetes mellitus and arterial hypertension (AHT). * To determine the improvement in quality of life by means of an accredited test.

Null hypothesis:

1\. There are no differences in muscle mass and bone density in patients who undergo supervised physical exercise postoperatively versus patients who do not exercise.

Alternative hypothesis:

1\. There are differences in muscle mass and bone density in patients undergoing supervised physical exercise postoperatively versus non-exercising patients.

Trial design The trial will consist of a randomised controlled study of patients currently on the surgical waiting list for bariatric surgery who meet the inclusion criteria until the sample size is completed.

Two groups (control and intervention) will be established and will come in waves.

Methods Participants, interventions and results Scope of the study The assessment and intervention of the study will take place at the Pablo de Olavide University in Seville. The medical assessment and surgical intervention will be carried out at the General and Digestive System Surgery Management Unit of the Virgen del Rocío University Hospital in Seville.

Вмешательства

  • Поведенческое physical exercise programme
    patients undergoing bariatric surgery who have undergone a post-operative supervised physical exercise programme and no exercise programme.

Первичные конечные точки

  • Differences in muscle mass [Срок оценки: 12 months]

Критерии участия

Критерии включения

Patients who are on the waiting list for bariatric surgery (gastric bypass or sleeve) at the Hospital Universitario Virgen del Rocío in Seville, in addition to:

  • Be 18 years of age or older.
  • Suitable for physical exercise.
  • Signature of informed consent. EXCLUSION CRITERIA.
  • Body weight greater than 150kg.
  • Distance from the place of residence to the Pablo de Olavide University in Seville greater than 60 km or 45 minutes by car.
  • Having any of the following conditions: lipedema, cancer survivors, metabolic bone diseases, consumption of medication or presence of pathology that affects bone health.
  • Patients undergoing dialysis.

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Рандомизированное
Модель
Параллельные группы
Маскирование
Открытое
Основная цель
Лечение

Центры проведения

Испания · 2 центра
  • Hospital virgen del rocio — Seville
  • Universidad Pablo de Olavide — Seville

Идентификаторы

NCT: NCT07324447 · OBEFIT STUDY

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗