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Набор скоро начнётся NCT07208435

Web-Based Exercise Program for Non-Specific Low Back Pain

Без фазы С лечением Non-specific Low Back Pain (NSLBP)

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: Web-Based Therapeutic Exercise Program, Traditional Home Exercise Program.
Кому может быть актуально
Состояния в реестре: Non-specific Low Back Pain (NSLBP). Базовые параметры: 18 лет — 45 лет · Все.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
Turkey (Türkiye)
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

Effectiveness of Web-Based Exercise Programs in the Management of Non-Specific Low Back Pain: A Randomized Controlled Trial

Обзор

This study evaluates the effectiveness of a web application-based exercise program (delivered via Physitrack) for managing non-specific low back pain (NSLBP) compared to traditional home exercise programs. The trial focuses on whether web-based delivery can improve pain, function, quality of life, and adherence, providing evidence for digital rehabilitation as a practical alternative to conventional physiotherapy.

Подробное описание

Non-specific low back pain (NSLBP) is a prevalent condition associated with pain, functional limitations, and reduced quality of life. Access to in-person physiotherapy can be limited by geographic, financial, or time-related constraints. Web-based exercise programs offer an accessible alternative by delivering personalized exercises, educational content, reminders, and self-monitoring tools via digital platforms.

This study aims to investigate whether a structured web application-based exercise program can improve outcomes for adults with NSLBP compared to traditional home exercises. The trial addresses gaps in current evidence regarding the effectiveness of telerehabilitation, patient engagement, and delivery modes, and seeks to determine if digital interventions can serve as a viable complement or alternative to conventional physiotherapy.

Вмешательства

  • Поведенческое Web-Based Therapeutic Exercise Program
    Participants complete an 8-week web-based therapeutic exercise program via Physitrack, with 30-45 minute sessions twice weekly. The program targets core strengthening, spinal mobility, posture correction, and pain reduction. Exercises progress weekly from basic core engagement and breathing techniques to advanced trunk control, dynamic movements, and integration. The platform provides instructional videos, reminders, educational content, and self-monitoring tools to enhance adherence, engagement
  • Поведенческое Traditional Home Exercise Program
    Participants follow a 6-week traditional home exercise program with 30-40 minute sessions, twice weekly. The program focuses on flexibility, basic trunk and core strengthening, balance, and ergonomic practice. Exercises progress weekly, including cat-cow stretches, pelvic tilts, glute bridges, partial curl-ups, bird-dog, lunges, and posture training. Participants perform exercises independently at home using printed instructions, aiming to reduce pain, improve spinal mobility, and enhance functi

Первичные конечные точки

  • Pain Reduction (Numeric Pain Rating Scale, NPRS) [Срок оценки: Baseline and 6 weeks after intervention]
Вторичные конечные точки (4)
  • Functional Disability (Oswestry Disability Index, ODI) [Срок оценки: Baseline and 6 weeks after intervention]
  • Quality of Life (Short Form Health Survey, SF-36) [Срок оценки: Baseline and 6 weeks after intervention]
  • Patient Satisfaction Questionnaire (PSQ) [Срок оценки: 6 weeks end of intervention]
  • Proprioception (Joint Position Sense Test, JPS) [Срок оценки: Baseline and 6 weeks after intervention]

Критерии участия

Критерии включения

  • Adults aged 18-45 years diagnosed with non-specific low back pain (NSLBP) for 6 weeks to <12 months.
  • Self-reported pain intensity ≥3 on a 0-10 Numeric Pain Rating Scale (NPRS).
  • Evidence of functional limitation (Oswestry Disability Index or Roland-Morris Disability Questionnaire).
  • Access to a smartphone, tablet, or computer with internet connectivity.
  • Ability and willingness to participate in telerehabilitation programs.

Критерии исключения

  • Specific causes of low back pain (herniated disc with radiculopathy, spinal stenosis, spondylolisthesis, fractures, infections, malignancy).
  • Neurological deficits (e.g., severe motor weakness, progressive neurological symptoms).
  • Severe psychiatric or cognitive disorders interfering with participation.
  • History of spinal surgery within the last year.
  • Severe comorbidities contraindicating exercise (e.g., uncontrolled diabetes, cardiovascular disease).
  • Pregnant or planning pregnancy during the study period.
  • Active substance or alcohol abuse.
  • Participation in other structured rehabilitation or physical therapy programs within the last 3 months.

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Рандомизированное
Модель
Параллельные группы
Маскирование
Открытое
Основная цель
Лечение

Центры проведения

Turkey (Türkiye) · 1 центр
  • Istanbul Medipol University — Istanbul

Публикации

  • Searle A et al., 2015
  • Hayden JA et al., 2005
  • Qaseem A et al., 2017
  • Fernández-Rodríguez R et al., 2021
  • Natour J et al., 2015
  • Wells C et al., 2014
  • Ware JE Jr, Sherbourne CD. The MOS 36-item short-form health survey (SF-36). I. Conceptual framework and item selection. Med Care. 1992 Jun;30(6):473-83. PMID 1593914
  • Fairbank JC, Pynsent PB. The Oswestry Disability Index. Spine (Phila Pa 1976). 2000 Nov 15;25(22):2940-52; discussion 2952. doi: 10.1097/00007632-200011150-00017. PMID 11074683

Идентификаторы

NCT: NCT07208435 · E-10840098-202.3.02-3388

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗