Contrology Training in Patients With Non-Specific Neck Pain

Официальное название

Effects of Contrology Training on Pain, Cervical Range of Motion, Disability, and Craniovertebral Angle in Patients With Non-Specific Neck Pain

Обзор

This randomized controlled trial will evaluate the effects of a 12-week Contrology training program in patients with non-specific neck pain. Participants will be randomly allocated into two groups. The experimental group will receive Contrology training, while the control group will receive conventional physiotherapy. Outcomes will include pain intensity, cervical range of motion, neck-related disability, and craniovertebral angle. Assessments will be performed at baseline, 4 weeks, 8 weeks, and 12 weeks. The study aims to determine whether Contrology training is more effective than conventional physiotherapy in improving pain, posture, mobility, and functional disability in adults with non-specific neck pain.

Подробное описание

Non-specific neck pain is a common musculoskeletal condition that may lead to pain, restricted cervical movement, functional disability, and altered head and neck posture. Forward head posture, commonly assessed through craniovertebral angle, is frequently associated with neck pain and may contribute to increased mechanical load on cervical structures. Exercise-based rehabilitation is commonly used for the management of non-specific neck pain; however, the effects of Contrology training on pain, cervical range of motion, disability, and craniovertebral angle require further investigation.

This study is designed as a single-center, two-arm, parallel-group randomized controlled trial. A total of 40 participants with non-specific neck pain will be recruited and randomly allocated into two equal groups. Group A will receive Contrology training, and Group B will receive conventional physiotherapy. The intervention period will be 12 weeks. Participants will be assessed at baseline, 4 weeks, 8 weeks, and 12 weeks.

The primary outcome will be craniovertebral angle, measured using standardized lateral-view digital photography. Secondary outcomes will include pain intensity measured by the Numeric Pain Rating Scale, neck-related disability measured by the Neck Disability Index, and cervical range of motion measured using a digital inclinometer and/or universal goniometer. The study will compare changes within each group over time and between groups to determine the effectiveness of Contrology training compared with conventional physiotherapy.

These points match your thesis protocol: randomized trial, 40 participants, Contrology versus conventional physiotherapy, and outcomes including NPRS, NDI, CVA, and cervical ROM assessed across baseline, 4, 8, and 12 weeks.

Вмешательства

• Другое Contrology Training
  Contrology training is a Pilates-based exercise program emphasizing concentration, control, centering, breathing, precision, and flowing movement. Participants will perform supervised exercises targeting postural correction, cervical and thoracic mobility, deep cervical flexor activation, scapular stabilization, core control, and controlled breathing for 12 weeks.
• Другое Conventional Physiotherapy
  Conventional physiotherapy will include routine exercise-based management for non-specific neck pain, including cervical range of motion exercises, stretching, strengthening exercises, postural correction, and patient education. Treatment will be provided for 12 weeks.

Первичные конечные точки

• Craniovertebral Angle [Срок оценки: Baseline, 4 weeks, 8 weeks, and 12 weeks]

Вторичные конечные точки (3)

• Numeric Pain Rating Scale [Срок оценки: Baseline, 4 weeks, 8 weeks, and 12 weeks]
• Neck Disability Index [Срок оценки: Baseline, 4 weeks, 8 weeks, and 12 weeks]
• Cervical Range of Motions [Срок оценки: Baseline, 4 weeks, 8 weeks, and 12 weeks]

Критерии участия

Критерии включения

• Inclusion Criteria:
• Adults aged 18 to 40 years.
• Participants diagnosed with non-specific neck pain.
• Neck pain duration of at least 4 weeks.
• Numeric Pain Rating Scale score of at least 3 out of 10.
• Craniovertebral angle less than 49 degrees.
• Participants willing to provide informed consent and attend the treatment sessions.

Критерии исключения

• Cervical radiculopathy or myelopathy.
• Cervical spinal stenosis.
• History of cervical spine fracture, trauma, or surgery.
• Inflammatory joint disease or systemic rheumatologic disorder.
• Neurological disorders affecting neck movement or posture.
• Vestibular disorders or severe balance problems.
• Any serious medical condition preventing participation in exercise-based treatment.
• Current participation in another neck pain rehabilitation program.

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

Двойное слепое

Основная цель

Лечение

Центры проведения

Пакистан · 1 центр

• Maqbool memorial hospital, Shakargarh. — Shakargarh

Идентификаторы

NCT: NCT07725978 · F24C14G30031 (Ailia Abbas)

Первоисточники (государственные реестры)

• ClinicalTrials.gov (NIH, США)

Открыть это исследование на ClinicalTrials.gov ↗