NCT07480746

Brief Summary

This study aims to compare the effectiveness of Bowen Therapy and Post-Isometric Relaxation Technique (PIRT) in the management of Text Neck Syndrome, a musculoskeletal condition caused by prolonged forward head posture during mobile phone or screen use. The study follows a randomized clinical trial design, ensuring that participants are randomly assigned to either the Bowen Therapy group or the PIRT group to minimize bias. The total study duration is nine months, including a six-week treatment phase and a three-week follow-up period. Assessments will be conducted at baseline, mid-intervention (3 weeks), post-intervention (6 weeks), and follow-up (9 weeks) to evaluate the short-term and sustained effects of both interventions. A consecutive sampling technique will be used, and participants who meet the inclusion and exclusion criteria will provide informed written consent before enrollment. The sample size was determined using G\*Power software (v3.1.9.7), based on previous research (Seemal et al., 2022), with an assumed large effect size (d = 1.0), α = 0.05, and 80% power. After accounting for a 20% attrition rate, a total of 42 participants (21 per group) will be included in the study. Overall, this study seeks to provide evidence on which therapeutic approach-Bowen Therapy or Post-Isometric Relaxation-is more effective in reducing pain, improving range of motion, and enhancing posture in individuals with Text Neck Syndrome.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
42

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Dec 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

November 17, 2025

Completed
24 days until next milestone

Study Start

First participant enrolled

December 11, 2025

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 11, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

February 11, 2026

Completed
1 month until next milestone

First Posted

Study publicly available on registry

March 18, 2026

Completed
Last Updated

March 20, 2026

Status Verified

March 1, 2026

Enrollment Period

2 months

First QC Date

November 17, 2025

Last Update Submit

March 17, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • Change in Neck Pain Intensity Measured by the Numeric Pain Rating Scale

    Neck pain intensity will be assessed using the Numeric Pain Rating Scale (NPRS), an 11-point self-reported scale ranging from 0 (no pain) to 10 (worst imaginable pain). Participants will rate their average neck pain over the previous 24 hours by selecting a number from 0 to 10. The primary outcome is the change in NPRS score from baseline to 6 weeks, with higher scores indicating greater pain intensity and lower scores indicating improvement.

    Baseline and 6 weeks (post-intervention)

Study Arms (2)

Bowen Therapy Group

EXPERIMENTAL

Participants in this group will receive Bowen Therapy after baseline assessment of forward head posture, cervical range of motion, pain intensity, and functional limitation. The intervention will consist of three sessions per week for six weeks (total 18 sessions), each lasting approximately 30-45 minutes. A standardized Bowen Therapy protocol will be applied, focusing on the cervical and upper back/shoulder regions. Techniques include gentle rolling moves with the therapist's thumb over the sternocleidomastoid (SCM), scalenes, suboccipitals, upper trapezius, levator scapulae, and pectoralis muscles, performed while the patient is in prone or seated position. The procedure incorporates short pauses between moves to facilitate neuromuscular integration.

Other: Bowen therapyOther: Post-Isometric Relaxation Technique (PIRT)

Post-Isometric Relaxation Technique Group

ACTIVE COMPARATOR

Participants in this group will receive Post-Isometric Relaxation Technique (PIRT) sessions, administered three times per week for six weeks (total 18 sessions), each lasting 30-45 minutes. The intervention involves the standardized application of PIRT on upper trapezius, sternocleidomastoid, levator scapulae, suboccipital, scalene, and pectoralis muscles. Each muscle will be positioned at its resistance barrier, and participants will perform a 5-10 second, 20% effort isometric contraction against therapist resistance, followed by 2-3 seconds of relaxation and gentle stretch toward the new barrier. The process will be repeated 3-5 times per muscle.

Other: Bowen therapyOther: Post-Isometric Relaxation Technique (PIRT)

Interventions

Participants will receive Bowen Therapy sessions three times per week for six weeks. Gentle rolling moves will be applied to the cervical and upper back muscles to reduce pain, muscle tension, and improve posture.

Bowen Therapy GroupPost-Isometric Relaxation Technique Group

Participants will undergo PIRT sessions three times per week for six weeks, involving gentle isometric contractions and relaxation of targeted neck and shoulder muscles to improve flexibility and reduce discomfort.

Bowen Therapy GroupPost-Isometric Relaxation Technique Group

Eligibility Criteria

Age18 Years - 35 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Adults aged between 18 to 35 years, inclusive of both genders. Craniovertebral angle less than 50 degrees indicating forward head posture. Self-reported neck pain onset or worsening associated with screen use e.g. pain and stiffness during or after prolonged device use.
  • Neck pain intensity of at least 4 to 7 on Numeric Pain Rating Scale. Daily screen time of ≥4 hours per day including smartphones, tablet, laptop, and desktop use for at least 5 days per week.

You may not qualify if:

  • Cervical radiculopathy or myelopathy. History of Cervical Spine Surgery. Recent (within three months) trauma to neck or shoulder region. Diagnosis of fibromyalgia, rheumatoid arthritis or any other inflammatory joint condition.
  • Ongoing treatment for neck pain from another healthcare provider. Neurological conditions affecting muscle tone or coordination. Severe postural abnormalities from congenital conditions.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

UIPT, UOL, Lahore

Lahore, Pakistan

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

November 17, 2025

First Posted

March 18, 2026

Study Start

December 11, 2025

Primary Completion

February 11, 2026

Study Completion

February 11, 2026

Last Updated

March 20, 2026

Record last verified: 2026-03

Locations