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Blood Flow-restricted Resistance Exercise to Promote Muscle Strength and Use in Adults With Incomplete Spinal Cord Injury

Blood Flow-restricted Resistance Exercise to Promote Muscle Strength and Use in Adults With Incomplete Spinal Cord Injury

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06907381
Enrollment
10
Registered
2025-04-02
Start date
2025-04-01
Completion date
2026-06-24
Last updated
2026-06-25

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

Conditions

Spinal Cord Injury Cervical

Keywords

Blood flow-restricted resistance exercise, Physical therapy, Rehabilitation, Electrical stimulation

Brief summary

Recovery of arm and hand motor control is critical for independence and quality of life following incomplete spinal cord injury (iSCI). Blood flow-restricted resistance exercise (BFRE) has emerged as a potential treatment addressing this need, but treatment guidelines and research reporting effectiveness are sparse. The purpose of this work is to provide case reports of people with cervical iSCI who use BFRE supplemented by electrical stimulation (ES) to increase the strength and functional use of selected upper extremity muscles.

Interventions

BEHAVIORALBlood flow-restricted resistance exercise

Participants will engage in baseline measurement of blood pressure, strength of target muscle contractions, and level of support needed for functional task performance. They will then begin BFRE treatment supplemented by electrical stimulation, if needed, two times weekly. Each exercise session will include performance of four sets of 20 repetitions of target muscle contraction on each side of the body followed by functional task performance.

Sponsors

Quality Living, Inc.
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
19 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Incomplete cervical spinal cord injury * Resting blood pressure between 80/50 mmHg and 150/90 mmHg for at least three consecutive days * Native speaker of English

Exclusion criteria

* Recent history of deep vein thrombosis or cardiovascular disease including uncontrolled hypertension or a blood-clotting disorder * Routine experience of orthostatic hypotension as defined as a drop in systolic/diastolic blood pressure greater than 20/10 mmHg when engaging in physical activity * Severe cognitive, communication, or behavioral disorder as determined by treatment team

Design outcomes

Primary

MeasureTime frameDescription
Change in muscle strengthBaseline and end of treatment at a maximum of 6 monthsChange in strength of target muscle(s) contraction as measured in pounds of force using a dynamometer.

Secondary

MeasureTime frameDescription
Change in number of repetitions of unassisted target muscle(s) contractionsBaseline and end of treatment at a maximum of 6 monthsTally of the number of target muscle contractions participant can perform during a single treatment session (80 repetitions max) without BFRE or electrical stimulation assistance.
Change in support required to perform functional taskBaseline and end of treatment at a maximum of 6 monthsProfessional assessment using the 7-point Functional Independence Measure (1 = total assistance; 7 = complete independence) to rate the level of support a participant requires to perform a functional task.
Change in perceived exertion when performing a functional taskBaseline and end of treatment at a maximum of 6 monthsParticipants will use the Borg category-ratio 10 Rating Exertion scale (0 = no exertion; 10 = highest level of effort) to rate the effort they expend to perform a functional task.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORSara Waid, DPT

Quality Living, Inc.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 26, 2026