- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT07848425
Postural Correction and Lumbar Stabilization vs MET for Postpartum Pain
Effects of Postural Correction Combined With Lumber Stabilization Exercises Versus Muscle Energy Technique in Post-partum Females
This randomized clinical trial will evaluate the effectiveness of combined postural correction and lumbar stabilization exercises compared with Muscle Energy Technique (MET) in postpartum women with sacroiliac joint dysfunction following cesarean delivery. The study will include women aged 18-45 years who are 12-48 weeks postpartum and meet the specified clinical criteria for sacroiliac joint dysfunction. A total of 82 participants will be randomly allocated into two groups of 41 participants each. The intervention group will receive postural correction and stabilization exercises, while the comparison group will receive Muscle Energy Technique. Treatment will be provided three times per week for four weeks. Pain intensity, functional disability, and pelvic girdle-related pain and activity limitations will be assessed using the Visual Analogue Scale (VAS), Oswestry Disability Index (ODI), and Pelvic Girdle Questionnaire (PGQ), respectively. Outcomes will be assessed before and after the intervention to determine the comparative effects of the two physiotherapy approaches.
연구 개요
상태
정황
연구 유형
등록 (추정된)
단계
- 해당 없음
참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
설명
Inclusion Criteria:
- Females aged 18-45 years. Postpartum women within the specified postpartum period according to the study protocol.
Participants who have postpartum low back/pelvic musculoskeletal symptoms relevant to the study.
Participants who are medically stable and able to participate in physiotherapy. Participants who are able to understand and follow verbal and written instructions.
Participants willing to participate in the study and provide written informed consent.
Exclusion Criteria:
- Women with a history of major spinal, pelvic, or lower-limb surgery. Participants with serious spinal pathology, including fracture, malignancy, infection, or severe neurological involvement.
Participants with severe cardiovascular, neurological, or systemic conditions that contraindicate therapeutic exercise or manual therapy.
Participants with acute musculoskeletal injury requiring medical/surgical management.
Participants with pregnancy-related complications requiring specialized medical management.
Participants currently receiving another structured physiotherapy program targeting the same condition.
Participants unable to understand or follow the intervention or outcome-assessment procedures.
Participants who decline or withdraw informed consent.
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 하나의
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
|
활성 비교기: Muscle Energy Technique (MET)
|
A physiotherapy-based exercise intervention consisting of postural correction strategies and lumbar stabilization exercises designed to improve postural alignment, trunk stability, and functional outcomes in postpartum females. A manual physiotherapy intervention involving therapist-guided muscle energy techniques to address musculoskeletal dysfunction and improve mobility and functional outcomes in postpartum females. |
|
실험적: Postural Correction and Lumbar
|
A physiotherapy-based exercise intervention consisting of postural correction strategies and lumbar stabilization exercises designed to improve postural alignment, trunk stability, and functional outcomes in postpartum females. A manual physiotherapy intervention involving therapist-guided muscle energy techniques to address musculoskeletal dysfunction and improve mobility and functional outcomes in postpartum females. |
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Pain
기간: 8 weeks
|
Pain measured by VAS |
8 weeks
|
공동 작업자 및 조사자
연구 기록 날짜
연구 주요 날짜
연구 시작 (추정된)
기본 완료 (추정된)
연구 완료 (추정된)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
키워드
기타 연구 ID 번호
- Aina
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
미국 FDA 규제 기기 제품 연구
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .