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A Comprehensive corrective exercise program with and without soft tissue massage therapy on pain, functional mobility and quality of life among office syndrome patients

A Comprehensive corrective exercise program with and without soft tissue massage therapy on pain, functional mobility and quality of life among office syndrome patients

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20241119063780N1
Enrollment
34
Registered
2024-11-29
Start date
2024-01-30
Completion date
Unknown
Last updated
2025-01-08

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

Conditions

Myalgia in office syndrome refers to muscle pain caused by prolonged sitting, poor posture, and repetitive movements. It commonly affects the neck, shoulders, and back, leading to discomfort and stiffness.. Myalgia

Interventions

Intervention 1: Intervention group: The study involves participants randomly assigned to Group A, who will be received the Comprehensive corrective exercise program. This massage regimen will be comp

Sponsors

University of Lahore
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: Aged between 18-55 years Both male and female Participants diagnosed with having atleast one myofacial trigger point on trapezius muscle Participants who reported using a laptop for more than three hours daily Participants who have worked in an office setting or on a laptop for more than 1 year

Exclusion criteria

Exclusion criteria: Pregnancy Patients with history of motor vehicle accident Patients with Cervical & lumbar radiculopathies with or without neurological deficits Patients with degeneration of spine Patients with history of myofascial pain therapy within the mouth Patients with recent fracture/dislocation

Design outcomes

Primary

MeasureTime frame
The Numerical Pain Rating Scale (NPRS) is a segmented numeric version of the visual analog scale (VAS) in which a respondent selects a whole number (0–10 integers) that best reflects the intensity of his/her pain. The common format is a horizontal bar or line. Timepoint: 8th week. Method of measurement: The NPRS takes <1 minute to complete Scores range from 0-10 points, with higher scores indicating greater pain intensity. The NPRS can be administered verbally (therefore also by telephone) or graphically for self-completion.;The BPI-sf is a modification of the Brief Pain Inventory - Long Form, which includes additional questions on demographics (date of birth, marital status, education, employment), pain history, aggravating and easing factors, treatment and medication, pain quality, and response to treatment. Timepoint: 8th week. Method of measurement: The Brief Pain Inventory - Short Form (BPI-sf) is a 9 item self-administered questionnaire used to evaluate the severity of a patient's pain and the impact of this pain on the patient's daily functioning. The patient is asked to rate their worst, least, average, and current pain intensity, list current treatments and their perceived effectiveness, and rate the degree that pain interferes with general activity, mood, walking ability, normal work, relations with other persons, sleep, and enjoyment of life on a 10-point scale.;The WHOQOL-BREF is a shorter version of the WHOQOL. Both were developed by the World Health Organization (WHO) and published in 1995. It has been tested for reliability and validity. The WHOQOL-BREF is a self-administered questionnaire comprising 26 questions on the individual's perceptions of their health and well-being over the previous two weeks. Timepoint: 8th week. Method of measurement: Responses to questions are on a 1-5 Likert scale where 1 represents "disagree" or "not at all" and 5 represents "completely agree" or "extremely". The WHOQOL-BREF covers four domains each with specific facets

Countries

Pakistan

Contacts

Public ContactHafsa Chandio

University of Lahore

Hafsaphysiotherapist0@gmail.com+92 302 3159237

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026