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Core Endurance Versus Segmental Stabilization Exercise in Recreational Athletes With Low Back Pain

2026년 8월 17일 업데이트: Doç.Dr.Ömer Şevgin, Uskudar University

Comparison of the Effects of Core Endurance Exercises and Segmental Stabilization Exercises on Low Back Pain and Core Endurance in Recreational Athletes With Non-Specific Low Back Pain: A Randomized Trial

Low back pain is a common musculoskeletal complaint among athletes, and most cases are classified as non-specific low back pain, in which no clear anatomical or pathological source of pain can be identified. Recreational athletes, who exercise regularly for health and fitness rather than for competition, often have less structured training planning and technical supervision than professional athletes, which may increase their susceptibility to musculoskeletal complaints. Core stability has become an important consideration in the prevention and management of low back pain. The core region includes the abdominal muscles, paraspinal muscles, diaphragm, and pelvic floor muscles, and plays an important role in maintaining spinal stability. Reduced activation and endurance of these muscles may increase the load on the lumbar spine and contribute to the development of low back pain. This randomized trial compares two exercise approaches in recreational athletes with non-specific low back pain: a core endurance exercise program and a segmental stabilization exercise program targeting the transversus abdominis and lumbar multifidus. Participants are randomly assigned to one of the two programs, both delivered three days per week for six weeks under physiotherapist supervision. Pain and functional status, dynamic balance, and core muscle endurance are assessed before the program and at the end of the six-week program.

연구 개요

상세 설명

Design and setting This is a two-arm, parallel-group randomized trial conducted at a sports club facility.

Institutional permission for the study site has been obtained. Participants Recreational athletes who have recently begun regular physical activity and who report non-specific low back pain are enrolled. Participants provide written informed consent after receiving detailed information about the purpose of the study, the tests to be performed, and the exercise protocol. Sampling and randomization Convenience sampling is used to identify eligible participants, followed by simple random allocation to one of the two exercise groups: the core endurance exercise group or the segmental stabilization exercise group. Allocation is 1:1. Interventions Both exercise programs are delivered three days per week for six weeks. Segmental stabilization group: exercises target the transversus abdominis and lumbar multifidus and comprise stabilization exercises in the quadruped position, transversus abdominis activation exercises in the supine position with the knees flexed, lumbar multifidus activation exercises in the prone position, and standing postural control exercises involving co-activation of the transversus abdominis and lumbar multifidus.

Core endurance group: exercises are performed under the supervision of a certified physiotherapist and comprise the front plank, the side plank, and the superman plank.

Each exercise consists of 20 repetitions with a 15-second isometric hold per repetition.

The set is repeated twice, with a 3-minute rest between sets. In the front plank the participant is supported on the forearms and toes, with the shoulders aligned over the elbows and the trunk and lower limbs maintained in a straight line, producing simultaneous activation of the abdominal and paraspinal muscles. In the side plank the participant is supported on one forearm with the body held in a straight line, the shoulder aligned with the elbow and the pelvis lifted from the floor, targeting the oblique muscles. In the superman plank the participant lies prone with the arms extended overhead and simultaneously lifts the upper and lower limbs from the floor, producing trunk extension and targeting the lumbar extensor muscles. Outcome assessment Assessments are performed at baseline (week 0) and at the end of the six-week program (week 6). Demographic information including age, sex, and sports history is recorded.

Functional status and pain are assessed with the Micheli Functional Scale, dynamic balance with the Star Excursion Balance Test, and core muscle endurance with clinical endurance tests. Variables The independent variable is the type of exercise program (core endurance exercises versus segmental stabilization exercises). The dependent variables are pain level, core muscle endurance, and dynamic balance performance. Statistical analysis Normality of distribution is assessed with histogram curves and the Shapiro-Wilk test, and homogeneity of variance with the Levene test. Parametric or non-parametric tests are selected accordingly. Analyses are performed with IBM SPSS Statistics 20. Independent samples t-tests are used to compare demographic characteristics between groups. Multivariate analysis of variance is used to evaluate between-group and within-group changes, with time (baseline and post-intervention measurements) as the within-subject factor and group as the between-subject factor. Where a statistically significant difference is found, post-hoc analyses are performed with the Tukey test. Change scores between groups are also compared with independent samples t-tests.

연구 유형

중재적

등록 (추정된)

60

단계

  • 해당 없음

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 연락처

연구 장소

      • Istanbul, 터키 (Türkiye)
        • 모병
        • Fitness club gym
        • 연락하다:
          • Armita Chitsaz
          • 전화번호: +905456052365

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

  • 성인

건강한 자원 봉사자를 받아들입니다

아니

설명

Inclusion Criteria:

  • Aged 18 years or older
  • Recreational athlete who has recently begun regular physical activity
  • Diagnosis of non-specific low back pain confirmed by an orthopaedic specialist
  • Two or more episodes of low back pain within the past year
  • Not participating in any other treatment program during the study period

Exclusion Criteria:

  • Radicular (nerve root) signs
  • Underlying systemic or visceral disease
  • Diagnosis of ankylosing spondylitis
  • Spinal pathology such as spondylolysis or spondylolisthesis
  • Previous lumbar spine surgery
  • History of vestibular dysfunction
  • Lower extremity injury within the past month
  • History of traumatic concussion within the past three months

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 무작위
  • 중재 모델: 병렬 할당
  • 마스킹: 하나의

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: Core endurance exercise
Participants perform a core endurance exercise program consisting of the front plank, the side plank, and the superman plank, three days per week for six weeks under physiotherapist supervision. Each exercise consists of 20 repetitions with a 15-second isometric hold, repeated for two sets with a 3-minute rest between sets.

Supervised isometric core endurance training comprising the front plank, side plank, and superman plank.

Each exercise: 20 repetitions of a 15-second isometric hold, two sets, 3-minute rest between sets. Three sessions per week for six weeks.

Supervised motor-control training targeting the transversus abdominis and lumbar multifidus, comprising quadruped stabilization, supine transversus abdominis activation with knees flexed, prone lumbar multifidus activation, and standing postural control with co-activation of both muscles. Three sessions per week for six weeks.
활성 비교기: Segmental stabilization exercise
Participants perform a segmental stabilization exercise program targeting the transversus abdominis and lumbar multifidus, three days per week for six weeks under physiotherapist supervision. The program comprises quadruped stabilization exercises, supine transversus abdominis activation with the knees flexed, prone lumbar multifidus activation, and standing postural control exercises involving co-activation of both muscles.

Supervised isometric core endurance training comprising the front plank, side plank, and superman plank.

Each exercise: 20 repetitions of a 15-second isometric hold, two sets, 3-minute rest between sets. Three sessions per week for six weeks.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Change in low back pain and functional status (Micheli Functional Scale)
기간: Baseline (week 0) and at the end of the six-week exercise program (week 6)
The Micheli Functional Scale is a five-item scale developed to assess low back pain related functional impairment and pain related changes in performance in athletes. It comprises one symptom question, three activity questions (extension, flexion, and jumping), and a visual analogue scale section. The symptom question is scored from 0 to 5; the activity questions are scored from 0 to 4 for extension, from 0 to 3 for flexion, and from 0 to 3 for jumping. The visual analogue scale section provides a 10-point assessment on a 10 cm line. The total score is calculated out of 25 and multiplied by 4 to produce a standardized score from 0 to 100. Lower scores indicate better functional status and higher scores indicate greater functional impairment.
Baseline (week 0) and at the end of the six-week exercise program (week 6)

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

스폰서

수사관

  • 연구 의자: Armita Chitsaz, Uskudar University

간행물 및 유용한 링크

연구에 대한 정보 입력을 담당하는 사람이 자발적으로 이러한 간행물을 제공합니다. 이것은 연구와 관련된 모든 것에 관한 것일 수 있습니다.

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (실제)

2026년 8월 15일

기본 완료 (추정된)

2026년 12월 1일

연구 완료 (추정된)

2026년 12월 30일

연구 등록 날짜

최초 제출

2026년 8월 7일

QC 기준을 충족하는 최초 제출

2026년 8월 7일

처음 게시됨 (실제)

2026년 8월 12일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 8월 18일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 8월 17일

마지막으로 확인됨

2026년 8월 1일

추가 정보

이 연구와 관련된 용어

키워드

기타 연구 ID 번호

  • Uskudar27
  • Uskudar University (기타 식별자: Non-Interventional Research Ethics Committee)

개별 참가자 데이터(IPD) 계획

개별 참가자 데이터(IPD)를 공유할 계획입니까?

아니요

IPD 계획 설명

Individual participant data will not be made publicly available. De-identified data supporting the findings may be made available from the corresponding author on reasonable request, subject to institutional approval.

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

아니

미국 FDA 규제 기기 제품 연구

아니

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. .

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