Ultrasound Muscle Biomarkers as Predictors of Isometric Quadriceps Muscle Strength and Handgrip i… (NCT07647393) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
Ultrasound Muscle Biomarkers as Predictors of Isometric Quadriceps Muscle Strength and Handgrip in Healthy Adults: an Observational Study
300 participantsStarted 2026-06
Plain-language summary
This observational study aims to determine whether ultrasound-derived muscle biomarkers can predict isometric quadriceps muscle strength and handgrip in healthy adults aged 18-89 years.
The main questions it aims to answer are:
* Which ultrasound muscle characteristics are associated with isometric quadriceps muscle strength and handgrip?
* Can ultrasound-derived biomarkers be used to develop predictive models of muscle strength in healthy adults?
Participants will undergo:
* Ultrasound assessment of the quadriceps and forearm flexor muscles;
* Measurement of isometric quadriceps muscle strength and handgrip using standardized dynamometry protocols;
* Assessment of functional capacity, mobility and balance;
* Completion of questionnaires related to health status, physical activity, nutrition, fatigue and health-related quality of life.
The study will also assess the reliability of ultrasound measurements and explore the relationship between ultrasound variables, muscle strength, physical function and health-related factors.
Who can participate
Age range
18 Years – 89 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Healthy adults aged 18-89 years.
* Resident in Spain for at least 5 years.
* Living independently in the community and able to complete all study assessments.
* Able to understand and follow verbal instructions in Spanish.
* Able and willing to provide written informed consent prior to study participation.
Exclusion Criteria:
* Neurological, musculoskeletal, or systemic disorders affecting muscle strength or mobility.
* Recent surgery or acute injury affecting the upper or lower limbs.
* Recent use of medications affecting the musculoskeletal system (e.g., systemic corticosteroids for \>1 week during the previous 6 months or muscle relaxants during the previous week).
* Cognitive or psychiatric conditions limiting participation.
* Pregnancy.
* Recent postpartum period (≤3 months after delivery).
* Presence of clinically relevant pain, fatigue, physical deconditioning, or functional limitations that may interfere with study procedures or measurement validity.
* Acute illness at the time of assessment.
* Uncontrolled hypertension (≥140/90 mmHg).
* Resting peripheral oxygen saturation ≤90%.
* Moderate-to-severe pain (Numeric Rating Scale ≥4/10).
* Any medical condition considered by the investigator to contraindicate study participation.
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.