NCT06801613

Brief Summary

Correlation Between Upper Cross Syndrome and Neck Proprioception Hypothesis: No statistically significant relationship exists between upper cross syndrome and neck proprioception. Study Design: Randomized Controlled Trial Participants: Office workers (≥4h computer use/day) Age: 28-48 years Chronic nonspecific neck pain (\>3 months) Forward head posture (FHP) \<46° VAS score: 3-8 cm No cognitive impairments affecting participation Exclusion Criteria: Systemic, rheumatic, or neuromuscular diseases Neurological signs, spinal surgery, or recent physical therapy Missing ≥3 consecutive or 4 nonconsecutive sessions

Trial Health

35
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
80

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started May 2025

Shorter than P25 for all trials

Status
not yet 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

First Submitted

Initial submission to the registry

January 25, 2025

Completed
5 days until next milestone

First Posted

Study publicly available on registry

January 30, 2025

Completed
3 months until next milestone

Study Start

First participant enrolled

May 1, 2025

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 25, 2025

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

October 25, 2025

Completed
Last Updated

January 31, 2025

Status Verified

January 1, 2025

Enrollment Period

3 months

First QC Date

January 25, 2025

Last Update Submit

January 29, 2025

Conditions

Keywords

proprioceptionupper cross syndromeneck

Outcome Measures

Primary Outcomes (1)

  • Cervical Proprioception:

    Measurement Tool: CROM device. Tests: Neutral Head Position (NHP): Assesses participants' ability to actively reposition their head to a self-selected neutral position. Target Head Position (THP): Assesses ability to reposition the head to a previously demonstrated target position.

    8 weeks

Secondary Outcomes (4)

  • Neck Pain

    8 weeks

  • Balance

    8 weeks

  • Neck Disability Index (NDI):

    8 weeks

  • Cervical Range of Motion (CROM)

    8 weeks

Other Outcomes (1)

  • Spinal Curvature:

    8 weeks

Study Arms (1)

control group

Participants with UCS who do not receive the intervention (e.g., may receive standard care, education, or no treatment).

Other: Intervention Group

Interventions

Group/Cohort Description: Participants with Upper Cross Syndrome (UCS) who undergo the prescribed exercise or treatment protocol.

control group

Eligibility Criteria

Age28 Years - 48 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)
Sampling MethodProbability Sample
Study Population

The study population consists of adult office workers with specific characteristics related to their occupation, posture, and neck pain history. Below is a detailed breakdown: Demographic Characteristics Age Range: 28-48 years. Gender: Not specified, but likely includes both males and females. Occupation: Office workers using computers for at least 4 hours daily. Clinical Characteristics Chronic Nonspecific Neck Pain (CNP): Pain lasting ≥3 months. Pain intensity between 3-8 cm on the Visual Analog Scale (VAS). Forward Head Posture (FHP): Measured angle of FHP is less than 46°. No Specific Diagnoses: Participants with neck pain due to systemic, rheumatic, or neuromuscular diseases are excluded.

You may qualify if:

  • office workers (using a computer at least 4 h),
  • aged between 28 and 48 years,
  • NP between 3 and 8 cm on a visual analog scale (VAS) (from 0 indicating no pain at all to 10 indicating unbearable pain),
  • chronic nonspecific neck pain lasting for more than 3 months, and FHP less than 46° (Fathollahnejad et al., 2019).
  • Patients willing and able to participate in an exercise program safely and without cognitive impairments that would limit their participation.

You may not qualify if:

  • specific causes of NP (e.g., systemic, rheumatic, neuromuscular diseases), central or peripheral neurological signs, cognitive impairment, spinal surgery, or physical therapy treatments in the last 6 months prior to the baseline assessment.
  • Participants would be also excluded if they missed at least three consecutive or four nonconsecutive sessions (Fathollahnejad et al., 2019).

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Oculocerebral hypopigmentation syndrome type Preus

Central Study Contacts

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Target Duration
8 Weeks
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
general practitioner

Study Record Dates

First Submitted

January 25, 2025

First Posted

January 30, 2025

Study Start

May 1, 2025

Primary Completion

July 25, 2025

Study Completion

October 25, 2025

Last Updated

January 31, 2025

Record last verified: 2025-01