Clinical trials

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Condition / disease
Location
Status: Not yet recruiting

Thoracic Expansion vs DNS Exercises in Forward Head Posture

This randomized controlled trial aims to compare the effects of thoracic expansion exercises and Dynamic Neuromuscular Stabilization (DNS) on respiratory function and bilateral trapezius muscle activity in individuals with forward head posture (FHP). A total of 32 participants aged 18-40 years with a craniovertebral angle (CVA) of less than 53° will be randomly assigned to either the DNS group or the thoracic expansion exercise group. Primary outcomes include respiratory function (FEV1, FVC, FEV1/FVC), trapezius muscle activation measured with EMG biofeedback, and craniovertebral angle. Secondary outcomes include thoracic mobility and health-related quality of life assessed using the St. George's Respiratory Questionnaire. Both interventions will be applied for 6 weeks. The study aims to determine which approach provides greater improvement in posture-related respiratory dysfunction and muscle activation.

Participants needed: 32
Trial details
Age: 18-40Biological sex: AllType: InterventionalSponsor: Esra BECENIUpdated: Nov 25, 2025Locations: 1
Eligibility criteria

Adults aged 18 to 40 years. [+4]

Contraindications to exercise (e.g., acute musculoskeletal injury, uncontrolled... [+6]

Status: Not yet recruiting

DNS vs Thoracic Stabilization Exercises in Thoracic Kyphosis

This randomized controlled trial aims to compare the effects of Dynamic Neuromuscular Stabilization (DNS) exercises and thoracic stabilization exercises on thoracic erector spinae muscle strength, thoracic kyphosis angle, pain and trunk stabilization in individuals with thoracic kyphosis. Thirty participants aged 18-40 years with thoracic kyphosis will be randomly allocated to a DNS exercise group or a thoracic stabilization exercise group. Surface EMG biofeedback will be used to assess thoracic erector spinae muscle activation, while pain, thoracic kyphosis angle and trunk endurance will be evaluated using validated clinical tests. The interventions will be applied for 6 weeks, and outcomes will be assessed before and after the intervention period.

Participants needed: 30
Trial details
Age: 18-40Biological sex: AllType: InterventionalSponsor: Esra BECENIUpdated: Dec 1, 2025Locations: 1
Eligibility criteria

Age between 18 and 40 years. [+4]

Age outside the range of 18-40 years. [+7]