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Automated Connective Tissue Torque Sensor

Automated Connective Tissue Torque Sensor

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01570647
Acronym
StromaTorque
Enrollment
165
Registered
2012-04-04
Start date
2012-02-29
Completion date
2013-01-31
Last updated
2013-10-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Connective Tissue, Musculoskeletal Pain

Brief summary

The purpose of this study is to develop a measure - the needle torque test - capable of detecting connective tissue abnormalities associated with musculoskeletal disorders.

Detailed description

Chronic musculoskeletal pain is a source of considerable disability, work absenteeism and health care costs. A major obstacle to the treatment of these conditions is the lack of methods to objectively assess connective tissues and measure the effect of treatments. Needle torque test technology under development in this project will potentially enable objective measurement of connective tissue abnormalities associated with musculoskeletal pain and dysfunction. This could help evaluate the efficacy of various treatments and enhance the objective monitoring of patient progress in clinical practice.

Interventions

None listed

Sponsors

National Center for Complementary and Integrative Health (NCCIH)
CollaboratorNIH
Stromatec, Inc.
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

for chronic low back pain subjects: * back pain that has disrupted activity for more than half the days in the past 12 months. Inclusion Criteria for restricted hamstring subjects: * 90/90 test of more than 20 degrees Inclusion Criteria for systemic scleroderma subjects: * physician diagnosis Inclusion criteria for joint hyperlaxity subjects: * Beighton test score of 7 or higher

Exclusion criteria

for all subjects: * surgery or scars in thighs or low back * neurological or major psychiatric disorder * bleeding disorders * acute systemic infection * pregnancy

Design outcomes

Primary

MeasureTime frame
Number of needle revolutions to achieve threshold torqueTime zero, 30 minutes and one week

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026