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An exploratory study of extracorporeal shockwave therapy to improve postpartum pelvic girdle pain and its mechanisms

An exploratory study of extracorporeal shockwave therapy to improve postpartum pelvic girdle pain and its mechanisms

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400082921
Enrollment
Unknown
Registered
2024-04-11
Start date
2024-04-11
Completion date
Unknown
Last updated
2024-04-15

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

Conditions

postpartum pelvic girdle pain

Interventions

The experimental group:The subjects received conventional treatment, mainly including general postpartum rehabilitation, such as manual traction and physiotherapy, for 20 minutes a day, 5 days a week,
The control group:The subjects received conventional treatment, mainly including general postpartum rehabilitation, such as manual traction and physiotherapy, for 20 minutes a day, 5 days a week, for

Sponsors

Shanghai Sixth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: ?The diagnostic criteria for postpartum pelvic belt pain are according to the diagnostic criteria of the British Medical Council Medical Journal 2011 updated pregnancy-related pelvic belt pain; ?Women at 6 weeks (approximately 42 days) ~6 months after delivery; ?Patients were aged between 18 and 45 years old; ?No history of lumbar spine trauma, fracture, or surgery; ?Postpartum related laboratory examination results did not show obvious abnormalities, excluding the interference of other factors; ?Volunteer to accept the clinical investigator.

Exclusion criteria

Exclusion criteria: ? Patients with malignant tumors; ? women with any pelvic belt and / or low back pain history before pregnancy ? severe cardiovascular and cerebrovascular diseases and other systemic diseases; ? with mental abnormalities, mental retardation can not actively cooperate with the training and treatment of patients ? Not meeting the treatment conditions and do not cooperate with the treatment.

Design outcomes

Primary

MeasureTime frame
pain scale;

Secondary

MeasureTime frame
Degree of pain and functional impairment;Degree of pain and functional impairment;Depression status/degree;Rectus abdominis width;Pelvic floor muscle strength assay;Kinematic indicators;

Countries

China

Contacts

Public ContactMan Wang

Shanghai Sixth People's Hospital

18801265163@163.com+86 188 0126 5163

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026