Evaluating the effects of exercise therapy on veterans' health
Evaluating the Impact of Focused Muscle Contraction Therapy in U.S. Veterans
NA · University of Illinois at Chicago · NCT05094297
This study tests whether a specific exercise program can help U.S. veterans with chronic pain, fatigue, and depression feel better physically and mentally.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 25 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University of Illinois at Chicago (other) |
| Locations | 1 site (Chicago, Illinois) |
| Trial ID | NCT05094297 on ClinicalTrials.gov |
What this trial studies
This study investigates the impact of the GH Method exercise program on body composition, physical abilities, and overall wellbeing in U.S. Veterans suffering from chronic pain, fatigue, and depression. Participants will undergo a total of 94 visits over 18 months, including fitness testing and exercise training sessions. The study aims to assess improvements in physical health and mental wellbeing through a structured exercise regimen and regular health evaluations.
Who should consider this trial
Good fit: Ideal candidates are U.S. Veterans experiencing pain, fatigue, or low energy levels who can commit to the exercise program.
Not a fit: Patients who are unable to travel to the training center or cannot comply with the training program may not benefit from this study.
Why it matters
Potential benefit: If successful, this program could significantly enhance the physical and mental health of veterans, leading to improved quality of life.
How similar studies have performed: Other studies have shown positive outcomes with exercise interventions for veterans, suggesting potential success for this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * U.S. Veterans * Eligible subjects must be patients at the Jesse Brown VA Medical Center and suffer from pain, fatigue, low energy levels or are unable to physically do things they were once able to do. * Subjects need to complete the PAR-Q with an acceptable score and/or must have written physician clearance. * 18 years of age and older Exclusion Criteria: * Unable to travel to the training center * Unable to give consent * Unable to understand the study * Unable to comply with the training program
Where this trial is running
Chicago, Illinois
- University of Illinois at Chicago — Chicago, Illinois, United States (RECRUITING)
Study contacts
- Principal investigator: Enrico Benedetti, MD — University of Illinois at Chicago
- Study coordinator: Ilaria Santi
- Email: isanti@uic.edu
- Phone: 312-996-4706
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Chronic Pain, Acute Pain, Fatigue, Depression