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Observation on the effect of comprehensive rehabilitation therapy on pelvic rotation syndrome

Observation on the effect of comprehensive rehabilitation therapy on pelvic rotation syndrome

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300069840
Enrollment
Unknown
Registered
2023-03-28
Start date
2023-04-01
Completion date
Unknown
Last updated
2023-05-29

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

Conditions

Pelvic rotation syndrome

Interventions

test group:Comprehensive rehabilitation techniques (release, chiropractic, functional training)
Control group:Chiropractic, functional training

Sponsors

Zhoushan Dinghai Guanghua Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria of pelvic rotation syndrome; 2. Age: 18~60 years old, gender unlimited; 3. Symptoms: lumbosacral pain with limited activity; 4. Physical signs: long and short legs, yin and yang feet, pelvis skew, lumbar scoliosis, positive four-word test of lower limbs, obvious tenderness of lumbosacral and iliac crest; 5. Imaging evaluation criteria: asymmetric hips on both sides (the upper edge line of the iliac crest on both sides is not on the same horizontal line, the width of the hip bones on both sides is not equal, the size of the obturator is asymmetric, etc.), and the pelvis is inclined; 6. The clinical data is complete and the informed consent is signed voluntarily.

Exclusion criteria

Exclusion criteria: 1. Congenital pelvic deformity; 2. Patients who have undergone major surgery, pregnant and lactating women, and those who are physically weak; 3. The researchers shall not collect or combine cardiovascular and cerebrovascular diseases, liver and kidney dysfunction, severe osteoporosis, bone tuberculosis and vertebral fusion patients with serious or even life-threatening diseases, such as AIDS, tumors, etc; 4. The disabled and mentally ill; 5. Those who are receiving other pelvic correction treatment or cannot cooperate with the treatment operator.

Design outcomes

Primary

MeasureTime frame
Visual analogue scoring(VAS));the MOS item short from health survey,(SF-36);

Secondary

MeasureTime frame
safety assessment;Pelvic plain film data;Four-character experimental abduction distance;

Countries

China

Contacts

Public ContactZhou Yuxiang

Dinghai Guanghua Hospital, Zhoushan City, Zhejiang Province

838084474@qq.com+86 15870855727

Outcome results

None listed

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