Menu
Recruiting NCT06552143

An Applied Study on the Use of Stone Needles Therapy to Assist the Rehabilitation of Maternal Diastasis Rectus Abdominis Based on the Theory of Belt Channel

No phase Interventional Diastasis Recti Abdominis

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Stone needle therapy follows the Belt channel.
Who it may be relevant to
Registry conditions: Diastasis Recti Abdominis. Basic parameters: 15 years — 49 years · Female.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
China
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

This clinical trial aims to find out whether stone needles therapy can effectively assist in the treatment of maternal diastasis rectus abdominis (DRA) based on the Belt channel theory, it will also validate whether the Ben-Tovim Walker body attitude questionnaire (BAQ) can be used as a tool to measure body image satisfaction in Chinese patients with postpartum DRA. The main questions it aims to answer are: Can stone needles therapy promote the recovery of maternal DRA? Whether the Chinese version of the Body attitude questionnaire (BAQ-C) can be used as a body image satisfaction measurement tool for patients with postpartum DRA. The researchers will add stone needles therapy to neuromuscular electrical stimulation (NMES) and massage therapy to see if stone needles therapy can promote the recovery of postpartum DRA.

Detailed description

Participants will: Receive NMES combined with massage therapy or the addition of stone needles therapy on a sub-basis every day for 10 days.

Abdominal circumference, inner rectus distance will be measured and recorded after each treatment Body imagery satisfaction, low back pain and dysfunction scores, anxiety, depression scores, and quality of life scores will be measured after all treatments are completed.

Interventions

  • Other Stone needle therapy follows the Belt channel
    Stone needle therapy follows the Belt channel involves the use of stones by the intervener to follow the path of the Belt channel by pushing and rubbing the abdomen of patients with postpartum diastasis rectus abdominis.

Primary outcome measures

  • inter-recti distance [Time frame: pre-intervention and after three stone needle therapies interventions]
  • Abdominal circumference [Time frame: pre-intervention and after three stone needle therapies interventions]
  • Body Image Satisfaction [Time frame: pre-intervention and after intervention]
Secondary outcome measures (5)
  • Low back pain Visual Analogue Scale [Time frame: pre-intervention and after intervention]
  • Oswestry Disability Index [Time frame: pre-intervention and measured immediately after completion of all treatments]
  • Self-Rating Anxiety Scale [Time frame: pre-intervention and measured immediately after completion of all treatments]
  • Edinburgh postnatal depression scale [Time frame: pre-intervention and measured immediately after completion of all treatments]
  • THE WORLD HEALTH ORGANIZATION QUALITY OF LIFE [Time frame: pre-intervention and measured immediately after completion of all treatments]

Eligibility criteria

Inclusion criteria

  • patients who meet the diagnostic criteria of postpartum rectus abdominis muscle separation, and the distance of rectus abdominis muscle separation is ≥3.0cm with postpartum low back pain.
  • Patients who are >42d postpartum and have cleaned up their discharge;
  • Women who are 42day-3 mouths after normal delivery;
  • Postpartum women who have not received any other treatment before treatment in our hospital;

Exclusion criteria

  • With severe parenchymal organ diseases such as renal, cardiac, or hepatic diseases or due to comorbid cognitive impairment, Alzheimer's disease or psychological or psychiatric diseases can not complete the cooperation, etc;
  • Those with contraindications to stone therapy;
  • Those with contraindications to bioelectric stimulation therapy.
  • Combined with puerperal infection and gastrointestinal adhesion;
  • Patients with postpartum back pain due to other reasons such as lumbar disc herniation or kidney stones;
  • Patients who cannot tolerate the program;

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Non-randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Treatment

Study locations

China · 1 center
  • YunNan Provincial Hospital of Traditional Chinese Medicine — Kunming

Identifiers

NCT: NCT06552143 · XW2023-025

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗