Arthropathies
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients of both genders. Adults aged 30 to 59 years. With musculoskeletal injuries (hip and knee). With a Body Mass Index of normal (18.5-24.9 kg/m 2 ) to overweight (24.9- 30kg/m2). Patients who had sleep disorders and/or insomnia. Patients who voluntarily agree to participate in the study and sign an informed consent form. Patients who are able to fulfill study requirements, such as keeping a sleep diary and regularly participating in rehabilitation sessions
Exclusion criteria
Exclusion criteria: Patients with a history of serious psychiatric disorders such as schizophrenia or bipolar disorder. Patients with severe neurological disorders such as Cerebrovascular Accident (CVA) or spinal cord injury. Patients with serious chronic illnesses such as Chronic Obstructive Pulmonary Disease (COPD) or Congestive Heart Failure (CHF). Patients who are using medications that affect sleep, such as benzodiazepines or antipsychotics. Patients who are pregnant or breastfeeding
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome of this study is to assess how sleep duration relates to clinical improvement in orthopedic patients during rehabilitation. We will employ statistical analysis to examine this, comparing sleep duration recorded by the actigraph with clinical assessments. The parameters include the average variation in sleep duration before and after rehabilitation, changes in scores from sleep and pain questionnaires, as well as an analysis of sleep patterns throughout the treatment. We anticipate discovering a connection between increased sleep duration and better clinical outcomes. Statistical analysis will determine the significance of these relationships, contributing to our research objectives | — |
Secondary
| Measure | Time frame |
|---|---|
| No secondary outcomes are expected. | — |
Countries
Brazil
Contacts
Universidade Estadual de Campinas