The Effect of Integrating a Smartphone Application with Global Postural Re-education on Cervical Proprioception in Patients with Upper Cross Syndrome
Trial Snapshot
- Phase
- Not Applicable
- Status
- Not yet recruiting
- Sponsor
- Cairo University
- Enrollment
- 50
- Primary Endpoint
- VAS (visual analogue scale)
Study Overview
Brief Summary
The Effect of Integrating a Smartphone Application with Global Postural Re-education on Cervical Proprioception in Patients with Upper Cross Syndrome
Design:
Randomized Controlled Trial (RCT).
Procedures:
Patients with cervical pain resulting from Upper Cross Syndrome (UCS), recruited from El Amal Clinic in Fayoum, will be randomly assigned to one of three groups:
Group A: Receives experimental interventions for 50 minutes per day, 4 days per week, over 8 weeks. The exercises are assisted by a smartphone application designed to support the intervention.
Group B: Receives the same interventions as Group A but without the use of the smartphone application. The exercises focus on stretching the anterior and posterior muscle chains.
Control Group: Receives conventional physiotherapy for 50 minutes per day, 4 days per week, over 8 weeks. This includes postural correction, neck education, and exercise therapy.
Inclusion Criteria:
Office workers aged between 28 and 48 years.
Chronic nonspecific neck pain with a Visual Analog Scale (VAS) score between 3 and 8.
Persistent pain for more than 3 months.
Absence of cognitive impairments and the ability to safely participate in an exercise program.
Postural changes characteristic of UCS, such as forward head posture and elevated shoulders.
Exclusion Criteria:
Specific causes of neck pain, such as systemic diseases or neurological signs.
History of spinal surgery or physical therapy treatments within the last 6 months.
Failure to attend three consecutive sessions or four non-consecutive sessions.
Instrumentation:
Assessment Tools:
Visual Analog Scale (VAS) to measure cervical pain.
Cervical Range of Motion (CROM) device to assess cervical range of motion and proprioception.
Neck Disability Index (NDI) to evaluate neck function.
Treatment Tools:
Smartphone application named "Kyphosis and Rounded Back."
Global Postural Reeducation methods.
Traditional physiotherapy techniques.
Detailed Description
The Effect of Integrating a Smartphone Application with Global Postural Re-education on Cervical Proprioception in Patients with Upper Cross Syndrome
Design:
Randomized Controlled Trial.
Participants:
The sample size will be determined using G power analysis.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Treatment
- Masking
- Double (Participant, Investigator)
Eligibility Criteria
- Ages
- 28 Years to 48 Years (Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •office workers(using a computer at least 4 h),
- •aged between 28 and 48years,
- •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 non specific neck pain lasting for more than 3 months (Fathollahnejad et al., 2019).
Exclusion Criteria
- •• 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 non consecutive sessions (Fathollahnejad et al., 2019).
Arms & Interventions
Group A: underwent the experimental interventions about 50 min a day, 4 days a week for an 8-week
Intervention: smartphone app exercises (Other)
• Group B: underwent the experimental interventions about 50 min a day, 4 days a week for an 8-week
• Group B: underwent the experimental interventions about 50 min a day, 4 days a week for an 8-week period.
Intervention: lying posture with progression (Other)
• control group: The participants in the performed an evidence-based physiotherapy program about 50
• control group: The participants in the performed an evidence-based physiotherapy program about 50 min a day, 4 days a week for an 8-week period, described as a postural correction on daily activities .
Intervention: Conventional physical therapy (Other)
Outcomes
Primary Outcomes
VAS (visual analogue scale)
Time Frame: 8 weeks
1. VAS (visual analogue scale) to assess cervical pain.
Secondary Outcomes
- Cervical ROM(8 weeks)
- Neck disability index (NDI)(8 weeks)
Investigators
Rania Ahmed
principal investigator
Cairo University