Acute Effects of Instrument-Assisted Soft Tissue Mobilization Added to Postural Corrective Exercises in Young Adults With Forward Head Posture
2 other identifiers
interventional
45
1 country
1
Brief Summary
This study investigated the acute effects of instrument-assisted soft tissue mobilization added to postural corrective exercises in young adults with forward head posture. Participants were randomly allocated to one of three groups: instrument-assisted soft tissue mobilization plus postural corrective exercises, postural corrective exercises only, or control. The primary outcome was craniovertebral angle. Secondary outcomes included cervical joint repositioning error, deep cervical flexor muscle endurance, and scapular muscle endurance. All outcomes were assessed at baseline and 1 hour after the intervention by a blinded outcome assessor.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started May 2024
1 active site
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
Study Start
First participant enrolled
May 22, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 22, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
June 18, 2025
CompletedFirst Submitted
Initial submission to the registry
May 19, 2026
CompletedFirst Posted
Study publicly available on registry
May 26, 2026
CompletedMay 26, 2026
May 1, 2026
1 year
May 19, 2026
May 19, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Craniovertebral Angle
Craniovertebral angle was assessed using digital photographic postural analysis. Markers were placed on the tragus of the ear and the spinous process of C7, and the angle was calculated from a lateral-view photograph. Higher values indicate a more upright head posture.
Baseline and 1 hour after the intervention
Secondary Outcomes (3)
Cervical Joint Repositioning Error
Baseline and 1 hour after the intervention
Deep Cervical Flexor Muscle Endurance
Baseline and 1 hour after the intervention
Scapular Muscle Endurance
Baseline and 1 hour after the intervention
Study Arms (3)
Instrument-Assisted Soft Tissue Mobilization Plus Exercise Group
EXPERIMENTALParticipants in this group received a single-session postural corrective exercise program and postural education in addition to instrument-assisted soft tissue mobilization applied to the cervicothoracic region.
Exercise Group
ACTIVE COMPARATORParticipants in this group received a single-session postural corrective exercise program and postural education.
Control Group
NO INTERVENTIONParticipants in this group received no intervention and were assessed at the same time intervals as the intervention groups.
Interventions
Participants received a single-session postural corrective exercise program and postural education in addition to instrument-assisted soft tissue mobilization. The exercise program included deep cervical flexor activation using the chin tuck exercise, active cervical range-of-motion exercises, scapular exercises, and pectoral stretching. Instrument-assisted soft tissue mobilization was applied bilaterally to the cervicothoracic region, including the upper and middle trapezius, sternocleidomastoid, levator scapulae, scalene, suboccipital, and cervical erector spinae muscles. The mobilization was applied for approximately 10 minutes using appropriate instruments.
Participants received a single-session postural corrective exercise program and postural education. The exercise program included deep cervical flexor activation using the chin tuck exercise, active cervical flexion, extension, lateral flexion and rotation exercises, scapular exercises, and pectoral stretching.
Eligibility Criteria
You may qualify if:
- Individuals aged 18-25 years
- Presence of forward head posture
- Provision of written informed consent
You may not qualify if:
- History of any disease or surgical procedure affecting cervical or thoracic posture
- Any health condition preventing completion of the assessments
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Dokuz Eylul University Faculty of Physical Therapy and Rehabilitation
Izmir, 35340, Turkey (Türkiye)
Study Officials
- STUDY CHAIR
Nihal Gelecek, Professor
Dokuz Eylul University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Masking Details
- Outcome assessments were conducted by an assessor who was blinded to group allocation. Due to the nature of the interventions, participants and the treating therapist could not be blinded.
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Research Assistant
Study Record Dates
First Submitted
May 19, 2026
First Posted
May 26, 2026
Study Start
May 22, 2024
Primary Completion
May 22, 2025
Study Completion
June 18, 2025
Last Updated
May 26, 2026
Record last verified: 2026-05
Data Sharing
- IPD Sharing
- Will not share
Individual participant data will not be shared because participant consent did not include public sharing of individual-level data.