Skip to content

Effects of Soft Tissue Mobilization on Postsurgical Adhesions, Pain, Lumbopelvic Muscle Functions, Spinal Mobility, and Posture in Postpartum Women With Caesarean Section

Effects of Soft Tissue Mobilization on Postsurgical Adhesions, Pain, Lumbopelvic Muscle Functions, Spinal Mobility, and Posture in Postpartum Women With Caesarean Section

Status
Suspended
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05008315
Enrollment
120
Registered
2021-08-17
Start date
2023-04-08
Completion date
2026-12-01
Last updated
2026-07-06

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

Conditions

Postsurgical Adhesion

Brief summary

Postpartum women with C-section receiving deep and superficial tissue mobilization would have better improvement on pain, lumbopelvic muscle functions, spinal mobility, and posture compare to the superficial tissue mobilization and control group

Interventions

OTHERMyofascial abdominal diaphragm release

Myofascial abdominal diaphragm release

OTHERDirect focused scar release technique

Direct focused scar release technique

OTHERDirect manipulations to visceral structures

Direct manipulations to visceral structures

pelvic anatomy education

OTHERsham

sham

Sponsors

YI-JU TSAI
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

vaginal delivery Inclusion Criteria: * Natural birth without C-section scar * Postpartum more than 6 months * Without any pain in the lumbopelvic region C-section Inclusion Criteria: * Healed C-section scar \> six months * Scar with or without pain Both mode of delivery

Exclusion criteria

* Active infection or infectious disease in the pelvis or abdomen * Pain medications on days of measurements * Skin irritation and inflammation at the site of the scar * Currently pregnant or actively trying to get pregnant * History of radiation to the area * Any fracture around spine and pelvis * Any previous gynecologic and obstetric surgery

Design outcomes

Primary

MeasureTime frameDescription
Scar Characteristic: Extensibility8 weeksThe extensibility of the scar will be measured using the modified adheremeter in each of 4 directions including superior, inferior, medial and lateral and then the area of mobility will be calculated.
Scar Characteristic: Viscoelasticity8 weeksThe biomechanical and viscoelastic properties of the scar tissue will be measured using a non-invasive myometer
Scar Characteristic: Irritability8 weeksThe irritability of the scar will be measured using the digital pressure algometer for two conditions: first, when the pressure turns from discomfort to pain and the participant asks to stop, and then when the maximal pressure or pain the participant can tolerate.
Muscle function measures of lumbopelvic muscles8 weeksUltrasonography image for muscle thickness of lumbopelvic muscles during rest and maximum contraction.
Muscle function measures of pelvic floor muscle control8 weeksUltrasonography image for muscle thickness of pelvic floor muscle control during rest, maximum contraction
Spinal Mobility8 weeksRange of motion for cervical, thoracic, and lumbar spine in the sagittal, frontal, and transverse plane as well as pelvic tilt will be assessed using the wireless double inclinometers
Myofascial Flexibility8 weeksStraight leg raise test and Thomas test will be used to examine the muscle flexibility of the major lower extremity muscles.
Spinal Alignment and Posture8 weeksRadiographic measurement, posture will be assessed using the photographic measurement. Reflective markers will first be placed and attached on the canthus of the eye, tragus of the ear, the spinous processes of C2, C7, T1, T3, T11, T12, L1, L5, S1, S5, and bilateral anterior superior iliac spine and posterior superior iliac spine in standing. The participants will be instructed to maintain their gaze straight ahead at a target adjusted for body height. Two standing photographs will be taken, one in the usual standing posture and the other in the best standing posture. Following the other two photographs will be taken, one in maximal pelvic anterior tilt and the other in the maximal pelvic posterior tilt.
Pain intensity measure of Visual Analogue Scale8 weeksVisual Analogue Scale is a self-reported instrument assessing average pain intensity in currently. Possible score range from 0 (no pain) to 10 (worst possible pain).
Pain intensity measure of pelvic girdle questionnaire8 weekspelvic girdle questionnaire is a self-reported instrument assessing pelvic girdle pain intensity in currently. Questionnaire consisting of 20 activity items and 5 symptom items on a 4-point response scale. Possible score range from 0 (no pain) to 100 (worst possible pain).
Pain intensity measure of Oswestry Low Back Pain Disability Questionnaire8 weeksOswestry Low Back Pain Disability Questionnaire is a self-reported instrument assessing patient's permanent functional disability in currently. For each section the total possible score is 5: if the first statement is marked the section score = 0; if the last statement is marked, it = 5. The higher the score, the greater the degree of disability.

Secondary

MeasureTime frameDescription
Self-perceived Change Health Status: Global Rating of Change Scale (GROC)8 weeksThe GROC is a single-item instrument that provides a means of measuring self-perceived change in health status. The GROC uses the 15-point Likert scale to rate the perceived "overall change" on a continuum, with -7 (labeled "worse") on the left and +7 (labeled "better") on the right, and 0 in the middle (labeled "no change"), compared with the baseline
Patient and Observer Scar Assessment Scale (POSAS)8 weeksThe POSAS includes 2 numerical numeric scales: The Patient Scar Assessment Scale and the Observer Scar Assessment Scale. It objectively assesses vascularity, pigmentation, thickness, relief, pliability, and surface area, and incorporates patient subjective symptoms of pain, itching, color, stiffness, thickness, and relief.

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 7, 2026