Comparing visual and pressure biofeedback for forward head posture
Comparative Effects of Visual and Pressure Biofeedback on Pain, Range of Motion and Disability in Symptomatic Forward Head Posture.
NA · Riphah International University · NCT06151951
This study is testing whether using visual or pressure feedback can help young and middle-aged adults with forward head posture reduce pain and improve their neck movement.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 28 (estimated) |
| Ages | 20 Years to 35 Years |
| Sex | All |
| Sponsor | Riphah International University (other) |
| Locations | 2 sites (Bahawalpur, Punjab and 1 other locations) |
| Trial ID | NCT06151951 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effects of visual and pressure biofeedback on pain, disability, and range of motion in young and middle-aged adults with forward head posture. Participants will be randomly assigned to two groups, one receiving pressure biofeedback and the other receiving visual biofeedback, both combined with isometric strengthening and stretching exercises. Each participant will undergo twelve treatment sessions over four weeks, with assessments conducted at the beginning and end of the treatment period to measure outcomes such as pain intensity and cervical range of motion.
Who should consider this trial
Good fit: Ideal candidates are young and middle-aged adults aged 20-35 who experience neck pain and have a specific craniovertebral angle.
Not a fit: Patients with neurogenic findings, severe metabolic diseases, or a history of significant spinal issues may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide effective non-invasive treatment options for individuals suffering from forward head posture.
How similar studies have performed: While there have been studies on biofeedback for postural correction, this specific comparative approach is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Participants would be complaining of neck pain as a primary complain and age of 20- 35 year was recruited in the study . 2 . Male and female both gender are included in the study. 3. patient with Craniovertebral angle (CVA)\<53 degree were included in the study . 4. Score more than 3 on NPRS and more than 10 on NDI. Exclusion Criteria: Participant failing to fall in this category would be excluded of the study. 1. Neurogenic findings like cervical trauma, myopathy, vestibular pathology, dizziness, visual problem, spinal Fracture, dislocation and hypertension will not include in the study. 2. History of sever metabolic diseases. 3. History of recurrent surgery in upper thoracic and lumber vertebrae 4. History of recent fractures in shoulder and neck region. 5. History of tumor. -
Where this trial is running
Bahawalpur, Punjab and 1 other locations
- Bahawal Victoria Hospital QAMC Bahawalpur — Bahawalpur, Punjab, Pakistan (RECRUITING)
- Bahawal Victoria Hospital QAMC Bahawalpur — Bahāwalpur, Punjab, Pakistan (RECRUITING)
Study contacts
- Principal investigator: Ali Raza — Riphah International University
- Study coordinator: Imran Amjid, PHD
- Email: imran.amlid@riphah.edu.pk
- Phone: +923324390125
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Forward Head Posture, FHP