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Role of Pressure Bio Feedback in Management of Forward Head Posture for Computer Users at BUMDC

Role of Pressure Bio Feedback in Management of Forward Head Posture for Computer Users at BUMDC

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05135741
Acronym
BUMDC
Enrollment
32
Registered
2021-11-26
Start date
2020-01-10
Completion date
2020-04-10
Last updated
2024-12-06

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

Conditions

Forward Head Posture

Keywords

Bio Feedback, Deep Cervical Flexor, Neck pain, Forward head posture, Neck Disability Index

Brief summary

Objective: The aim of present study is to explore the effectiveness of pressure bio feedback in treatment of occupational forward head posture on computer users.

Detailed description

Material & Methods: This Randomized Control Trial was conducted in Bahria University College of Physical Therapy, Karachi. Ethical approval was prior taken from Institute Review Board. there were 32 participants selected randomly equally in experimental and control group. Both male and female were included with age of 25 to 55 years currently employees of Bahria University (BUMDC) having forward head posture or complaining neck pain were included. Exclusion was age less than 25 years, history of cervical trauma or surgery, any neurological conditions or cervical pathology. Experimental Group was given DCF exercises with Pressure Biofeedback Unit (PBU) and Control Group was given Conventional DCF Exercises. SPSS version 23.0 was used for analysis.

Interventions

DEVICEpressure bio feedback

The pressure biofeedback unit was placed between the plinth and the posterior aspect of the neck just below the occiput and inflated to a baseline of 20 mmHg. A trained physiotherapist was observing and correcting any substitution movements to ensure that all subjects could perform the exercises correctly. All exercise protocols and programs were taken from previously published studies8-10. A conventional DCF exercise protocol was performed three times a week for four weeks in both groups. The duration of the conventional DCF exercise protocol was 20-30 minutes, once a day in the control group, and 15-20 minutes, once a day in the experimental group

Sponsors

Bahria University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
25 Years to 55 Years
Healthy volunteers
Yes

Inclusion criteria

\- Both male and female age of 25 to 55 currently employees of Bahria University (BUMDC) having forward head posture complaining neck pain.

Exclusion criteria

* Students of Bahria University history of cervical trauma or surgery any neurological conditions or cervical pathology

Design outcomes

Primary

MeasureTime frameDescription
change in range of cervical flexion15 minutes before and after exercises for 4 weekspre and post range of cervical flexion assessed through CROM device
change in range of right and left lateral rotations15 minutes before and after exercises for 4 weekspre and post right and left lateral rotations assessed through CROM device

Secondary

MeasureTime frameDescription
improvement in capacity of heavy weight lifting4 weekspre and post improvement in capacity of heavy weight lifting assessed through 6 kg dumbless
change in pain intensity4 weeks before exercise and 4 weeks after exercisespain was assesses pre and post using neck disability index (NDI)

Countries

Pakistan

Outcome results

None listed

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