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AI Training Program vs Standard Correction for Forward Head and Rounded Shoulder in Neck Pain

Artificial Intelligence Training Program Versus Standard Correction for Forward Head and Rounded Shoulder in Non-specific Neck Pain

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07236385
Acronym
AI
Enrollment
46
Registered
2025-11-19
Start date
2025-11-30
Completion date
2026-10-01
Last updated
2025-12-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Forward Head Posture, Rounded Shoulder Posture, Upper Cross Syndrome

Keywords

forward head and rounded shoulder posture ,hyperkyphosis OR thoracic kyphosis

Brief summary

this study will be to evaluate the effectiveness of AI-recommended exercise interventions versus standard corrective exercises in management of non-specific neck pain with forward head and rounded shoulder posture. with the goal of improving neck pain, functional disability, forward head, and rounded shoulder postures.

Detailed description

The aim of the current study is to evaluate the efficacy of APECS-AI app suggested exercises and standard corrective exercises in managing non-specific neck pain with forward head and rounded shoulders posture. Forty-six subjects of both genders between (18 and 35 years old) have non-specific neck pain with forward head and rounded shoulder posture will be enrolled in this study. The subjects will be randomized into two equal groups (n = 23 each): An intervention group (Group A), will receive AI-generated personalized exercise regimens from the APECS-AI app, and a control group (Group B), will perform standard corrective exercises

Interventions

OTHERAI based exercise

receive AI-generated personalized exercise regimens from the APECS-AI app

Each exercise session begins with 10 min of warm-up activity and ends with 5 min of cool-down. Selected exercises will be designed in two phases: first, and second phases. Exercises will be progressed in frequency and intensity during these phases

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 35 Years
Healthy volunteers
No

Inclusion criteria

Subjects with non-specific neck pain who had localized neck pain felt it anywhere along the cervical spine, from the superior nuchal line to the first thoracic spinous process. Neck pain between 3 and 8cm on a visual analogue scale. Subjects suffering from chronic (\> 12 weeks) neck pain. Subjects with forward head posture with craniovertebral angle (CVA) angle less than 50 degrees. Subjects with rounded shoulder posture as shoulder angle \< 52. Subjects must not have received any pharmacological medication related to their musculoskeletal condition as non-steroidal anti-inflammatory drugs or muscle relaxant for at least three months prior to enrolment in the study. Subjects must not have involved in any form of physical therapy or structured postural correction programs within the 6 months prior to study -

Exclusion criteria

1. Musculoskeletal diseases, cardiopulmonary diseases, and a history of surgery that could affect the experiment. 2. History of cervical spine injury or surgery. 3. Neck pain secondary to other conditions (e.g. Neoplasm, neurological diseases or vascular diseases). 4. Spondylosis and spondylolisthesis 5. A neurological disease, infection. 6. Inflammatory arthritis in the cervical spine. 7. Poor general health status that would interfere with the exercises -

Design outcomes

Primary

MeasureTime frameDescription
The craniovertebral angle6 weeksforward head posture. will be measured by Kinovea software and the APECS AI app. More than 50 degrees is considered normal.
Shoulder angle6 weeksrounded shoulder posture will be measured by Kinovea software and the APECS AI app. more than 52 is considered normal
functional disability6 weeksis measured by neck disability index (NDI). A higher score reflects a greater level of neck disorder-related disability
pain level6 weeksIt is measured by visual analogue scale (VAS). 10-cm line that represents a pain spectrum between no pain and worst pain, as the word descriptions no pain on the left and worst imaginable pain on the right serve as anchors for the 100-mm-long horizontal line

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026