NCT07182461

Brief Summary

Upper Crossed Syndrome (UCS) is a pattern of muscle imbalance that leads to forward head posture, rounded shoulders, or excessive thoracic kyphosis, thereby affecting posture and cervical-shoulder function. Dynamic Taping is a taping technique aimed at enhancing movement control and muscle support through its elastic material and tension, influencing the skin and neuromuscular system. When applied to UCS patients, Dynamic Taping can assist in posture correction, improve posture control, and increase scapular dynamic stability. Additionally, Dynamic Taping can enhance proprioception, helping patients maintain proper posture through sensory feedback. Corrective exercises improve posture and stability by strengthening weakened muscles and stretching tight muscles. Combining these two interventions is expected to help address poor posture.

Trial Health

77
On Track

Trial Health Score

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

Enrollment
36

participants targeted

Target at P25-P50 for not_applicable

Timeline
3mo left

Started Mar 2025

Geographic Reach
1 country

1 active site

Status
recruiting

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

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress83%
Mar 2025Jul 2026

Study Start

First participant enrolled

March 13, 2025

Completed
3 months until next milestone

First Submitted

Initial submission to the registry

June 11, 2025

Completed
3 months until next milestone

First Posted

Study publicly available on registry

September 19, 2025

Completed
10 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 15, 2026

Expected
16 days until next milestone

Study Completion

Last participant's last visit for all outcomes

July 31, 2026

Last Updated

September 19, 2025

Status Verified

September 1, 2025

Enrollment Period

1.3 years

First QC Date

June 11, 2025

Last Update Submit

September 17, 2025

Conditions

Keywords

posturemuscle imbalanceproprioception

Outcome Measures

Primary Outcomes (2)

  • Posture (CVA and SSA and Kyphosis Angle)

    The craniovertebral angle (CVA) and shoulder sagittal angle (SSA) were measured using the Physiomaster mobile application. During the measurement, the examiner positioned the smartphone to align the subject's image with the vertical and horizontal reference lines on the screen and then captured a photograph. The anatomical landmarks used for angle determination included the lateral canthus of the eye, the tragus of the ear, the spinous process of the seventh cervical vertebra (C7), and the midpoint of the line connecting the acromial processes. The thoracic kyphosis angle was measured using the Angle Meter mobile application. First, the device was calibrated to 0°. The smartphone was then placed at the level just inferior to T1 and subsequently at the level superior to T12. The kyphosis angle was calculated by summing the two measured angles.

    Participants were assessed at time points: prior to the intervention (baseline), immediately three weeks after the intervention, and at a one-month follow-up.

  • Cervical Proprioception

    Cervical proprioception was assessed using the Head Repositioning Accuracy (HRA) test with a cervical range of motion (CROM) device. Participants were instructed to adopt and recognize the neutral head position (0°). The head was then passively guided to 30° of flexion, extension, lateral flexion, and rotation. After each movement, participants actively returned to the perceived neutral position under both eyes-open and eyes-closed conditions. The repositioning error was defined as the angular difference between the actual and the perceived 0° position

    Participants were assessed at time points: prior to the intervention (baseline), immediately three weeks after the intervention, and at a one-month follow-up.

Study Arms (4)

Combined Dynamic Taping and Corrective Exercise (DT+EX Group)

EXPERIMENTAL

Participants in this group received postural taping using dynamic tape aimed at correcting forward head posture, rounded shoulders, and thoracic kyphosis. The tape was worn continuously throughout the intervention period, 24 hours a day. It was reapplied if participants reported detachment; otherwise, it was replaced every three days. In addition to taping, participants performed a corrective exercise program based on the NASM Corrective Exercise Continuum, which included four phases: inhibit, lengthen, activate, and integrate. The intervention lasted for three weeks, with 3 to 4 sessions per week, totaling 10 training sessions. Each session lasted approximately 60 to 75 minutes.

Device: Dynamic TapeDevice: Swiss BallDevice: DumbbellsDevice: Visual Feedback Laser Device

Dynamic Taping (DT Group)

ACTIVE COMPARATOR

Participants in this group received postural taping using dynamic tape aimed at correcting forward head posture, rounded shoulders, and thoracic kyphosis. The taping method was identical to that used in the DT + EX group. The tape was worn continuously throughout the intervention period, 24 hours a day. It was reapplied if participants reported detachment; otherwise, it was replaced every three days. The intervention lasted for three weeks. No corrective exercise intervention was provided to this group.

Device: Dynamic Tape

Corrective Exercise Group (EX Group)

ACTIVE COMPARATOR

Participants in this group performed only the corrective exercise component used in the DT + EX group. The program was based on the NASM Corrective Exercise Continuum and included four phases: inhibit, lengthen, activate, and integrate. The intervention lasted for three weeks, with 3 to 4 sessions per week, totaling 10 training sessions. Each session lasted approximately 60 to 75 minutes. No taping was applied to this group.

Device: Swiss BallDevice: DumbbellsDevice: Visual Feedback Laser Device

Control Group

NO INTERVENTION

Participants in this group did not receive any intervention. They were instructed to maintain their usual daily activities and lifestyle throughout the three-week study period.

Interventions

Dynamic Tape is a viscoelastic tape designed to assist movement and absorb load. The material is composed of either Nylon/Lycra or Recycled PET/Lycra.

Combined Dynamic Taping and Corrective Exercise (DT+EX Group)Dynamic Taping (DT Group)

A 75 cm diameter Swiss ball was used to provide an unstable surface during the exercise intervention.

Also known as: Therapy Ball
Combined Dynamic Taping and Corrective Exercise (DT+EX Group)Corrective Exercise Group (EX Group)
DumbbellsDEVICE

During the exercise intervention, 1 kg and 2 kg dumbbells were used as external resistance.

Combined Dynamic Taping and Corrective Exercise (DT+EX Group)Corrective Exercise Group (EX Group)

A headband was prepared to attach the laser pointer securely, allowing participants to wear it . This visual feedback laser device was used during proprioceptive training to provide real-time feedback.

Combined Dynamic Taping and Corrective Exercise (DT+EX Group)Corrective Exercise Group (EX Group)

Eligibility Criteria

Age20 Years - 35 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Age: \>20years
  • Craniovertebral angle (CVA) of \<48
  • Sagittal plane acromial angle of \<52°

You may not qualify if:

  • Allergic reactions to dynamic taping
  • Bodyweight outside the normal range (BMI between 18 and 25)
  • Any evident misalignment in the cervical spine, pelvis, or lower/upper limbs
  • Trunk rotation exceeding 5°during forward bending tests due to scoliosis
  • History of inherited muscle diseases, soft tissue lesions, or joint diseases involving the spine, scapulae, shoulders, abdomen, or pelvis
  • History of fractures or surgeries.
  • Inability to understand instructions

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Department of Physical Therapy of China Medical University

Taichung, Beitun, 406040, Taiwan

RECRUITING

MeSH Terms

Conditions

Oculocerebral hypopigmentation syndrome type Preus

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

June 11, 2025

First Posted

September 19, 2025

Study Start

March 13, 2025

Primary Completion (Estimated)

July 15, 2026

Study Completion (Estimated)

July 31, 2026

Last Updated

September 19, 2025

Record last verified: 2025-09

Locations