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Deep Fascial Mobilization for Tissue Adhesions

N/A
Waitlist Available
Research Sponsored by Rocky Mountain University of Health Professions
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up change from 0 weeks to 4 weeks to 8 weeks to 16 weeks
Awards & highlights

Study Summary

Over 1.37 million Caesarian sections (C-sections) are performed annually in the US . It is estimated that 12-20 % of those will result in chronic scar pain. This pain can lead to functional difficulties performing activities of daily living, pain with bowel movements, and pain with sexual activity . There is anecdotal evidence supporting the use of deep fascial scar mobilization techniques in reducing abdominal surgical scar pain, and yet almost no research has been published. The aims of this randomized clinical trial will be to determine if deep fascial scar mobilization techniques or superficial scar mobilization techniques will improve chronic pain and its resulting functional deficits, threshold pressure discomfort, pressure tolerance and mobility restrictions resulting from C-section surgery and to see if these interventions are more effective than no intervention. A positive result may result in an increase in the use of this intervention and thus the reduction of chronic scar pain for many women; it may provide justification for insurance reimbursement for this approach and it will also pave the way for further investigation into the use of these techniques with other types of painful scars including hysterectomy.

Eligible Conditions
  • Tissue Adhesions
  • Scar
  • Cesarean Section

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~change from 0 weeks to 4 weeks to 8 weeks to 16 weeks
This trial's timeline: 3 weeks for screening, Varies for treatment, and change from 0 weeks to 4 weeks to 8 weeks to 16 weeks for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Adheremeter
Digital Pressure Algometer
Secondary outcome measures
Global Rating of Change
Goniometery hip extension and shoulder flexion
Numeric Pain Rating Scale
+2 more

Trial Design

2Treatment groups
Experimental Treatment
Group I: Superficial Fascial MobilizationExperimental Treatment1 Intervention
Group II: Deep Fascial MobilizationExperimental Treatment1 Intervention

Find a Location

Who is running the clinical trial?

Rocky Mountain University of Health ProfessionsLead Sponsor
6 Previous Clinical Trials
430 Total Patients Enrolled
Franklin Pierce UniversityOTHER
15 Previous Clinical Trials
1,057 Total Patients Enrolled
Section on Women's Health American Physical Therapy AssociationUNKNOWN

Frequently Asked Questions

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~3 spots leftby May 2025