Clinical Trials Logo

Lumbago clinical trials

View clinical trials related to Lumbago.

Filter by:
  • Recruiting  
  • Page 1

NCT ID: NCT05923736 Recruiting - Osteoporosis Clinical Trials

Cardiovascular Risk in Digital Osteoarthritis

RICARDI
Start date: October 4, 2023
Phase: N/A
Study type: Interventional

The goal of this cross-sectional case control study is to investigate the cardiovascular risk in digital osteoarthritis. This study aims to compare the cardiovascular risk between group of patients with digital osteoarthritis and control group of patients with non-osteoarthritis disease paired by measurement of carotid intima-media thickness. All participants will undergo an ultrasound scan to measure carotid intima media thickness, a clinical assessment with the rheumatologist and a cardiovascular risk assessment.

NCT ID: NCT04725344 Recruiting - Chronic Disease Clinical Trials

Relevance of the Activ'Dos App for Chronic Low Back Pain Patients

ACTIV'DOS
Start date: July 26, 2021
Phase: N/A
Study type: Interventional

The purpose of this study is to compare a self rehabilitation program using ACTIV'DOS app versus using a standard sheet of paper.

NCT ID: NCT01155804 Recruiting - Anxiety Clinical Trials

Assessment of the Effectiveness of a Program of Preparation to Pregnancy and Delivery

Start date: June 2009
Phase: Phase 4
Study type: Interventional

Introduction: randomized studies on programs implemented during pre-natal care that offer information and physical activities preparing pregnant women for delivery are scarce in the scientific literature. Objective: to evaluate the effectively of the Program for Preparation of Pregnant Women for Delivery on the prevention of physical and psychological difficulties and problems during pregnancy and delivery in nulliparous women participating in the program. Subjects and methods: a randomized clinical single blind trial will be conducted with 192 pregnant nulliparous women allocated to participate or not of the program activities. The women allocated to the study group will participate of physical and educational activities at each pre-natal consultation and will receive orientation on the exercises they will perform at their home. Participants of the non-interventional group will follow the habitual routine care at the service. Participants will be selected among nulliparous low risk pregnant women aged between 16 and 40 years old after the 20th week of gestation. Data analysis: will be performing by intention to treat. For the continues variables the t-Student or Wilcoxon test will be performing; for the categorical variables the tests x² or Fisher, and the risk estimate will be estimated using a Relative Risk with 95% CI. ANOVA will be use for measures between the groups and along time, and correlation tests for anxiety and physical activity with gestational and perinatal variables.