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Self-Acupressure for Postpartum Low Back Pain Rehabilitation: An Application Study

Self-Acupressure for Postpartum Low Back Pain Rehabilitation: An Application Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400085579
Enrollment
Unknown
Registered
2024-06-12
Start date
2024-06-14
Completion date
Unknown
Last updated
2024-07-08

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

Conditions

postpartum low back pain

Interventions

Self acupressure: acupressure
health education:Health education for patients

Sponsors

Guangdong Hospital of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: (1) Meets the criteria for postpartum low back pain; (2) Low back pain occurred between 42 days and 2 years after delivery; (3) Aged 20-45 years; (4) No skin problems such as localised skin breakdown; (5) Voluntarily participate and sign an informed consent form after a full explanation of the purpose and procedures of this clinical trial, as well as any risks and potential adverse effects of this trial procedure

Exclusion criteria

Exclusion criteria: Those with one of the following conditions could not be included in this trial: (1) Patients with lumbar spine congenital sarcoidosis, spinal stenosis, narrow plate fracture, fracture, osteoporosis and other bony diseases; (2) Those who participated in other experimental interventions for low back pain symptoms within 2 weeks; (3) Pregnancy status or during the experiment pregnancy and family planning; (4) Malignant tumour, cancer pain metastasis, gynecological, urological, surgical, organ lesions or tuberculosis caused by low back pain; and (5) Suffering from serious heart, lung, brain, blood system diseases and diabetic patients; (6) Those who are unable to complete the basic course of treatment, have poor compliance and cannot adhere to the treatment according to the guideline and have difficulties in follow-up.

Design outcomes

Primary

MeasureTime frame
pain level;mental health;

Secondary

MeasureTime frame
Lumbar function;walking ability;range of motion of the trunk;quality of life;

Countries

China

Contacts

Public ContactJuanChen

Guangdong Hospital of Traditional Chinese Medicine

hlym@gzucm.edu.cn+86 134 3419 8780

Outcome results

None listed

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