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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05135741
Other study ID # ERC 12/2020
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 10, 2020
Est. completion date April 10, 2020

Study information

Verified date November 2021
Source Bahria University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 32
Est. completion date April 10, 2020
Est. primary completion date March 10, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 25 Years to 55 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Device:
pressure 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

Locations

Country Name City State
Pakistan BUMDC Karachi Sindh

Sponsors (1)

Lead Sponsor Collaborator
Bahria University

Country where clinical trial is conducted

Pakistan, 

Outcome

Type Measure Description Time frame Safety issue
Primary change in range of cervical flexion pre and post range of cervical flexion assessed through CROM device 15 minutes before and after exercises
Primary change in range of right and left lateral rotations pre and post right and left lateral rotations assessed through CROM device 15 minutes before and after exercises
Secondary improvement in capacity of heavy weight lifting pre and post improvement in capacity of heavy weight lifting assessed through 6 kg dumbless 4 weeks
Secondary change in pain intensity pain was assesses pre and post using neck disability index (NDI) 4 weeks before exercise and 4 weeks after exercises
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