Health Condition 1: M958- Other specified acquired deformities of musculoskeletal system
Conditions
Interventions
Intervention1: Comparing the Effect of Stretching and PNF in the management of Lower Cross Syndrome: Treatment Protocol
PNF Intervention Group
Control Group (Standard Care)
Frequency of Sessions
3 ti
Sponsors
GALGOTIAS UNIVERSITY
Eligibility
Inclusion criteria
Inclusion criteria: 1.Age Range: Office workers aged 25-50 years. 2.Diagnosis of lower Cross Syndrome (LCS): Confirmed by a physical therapist or medical professional based on clinical assessment and postural analysis. 3.Occupation: Individuals who spend at least 6 hours a day in a sedentary position, primarily working at a desk or computer. 4.Duration of Symptoms: Participants must have experienced symptoms of LCS, such as Back pain, hamstring tightness, or postural imbalances, for at least 3 months. 5.Willingness to Participate: Participants must be willing to attend regular sessions and follow the prescribed PNF intervention protocol. 6.Informed Consent: Participants must provide written informed consent to participate in the study.
Exclusion criteria
Exclusion criteria: History of Severe Musculoskeletal or Neurological Conditions: Excludes individuals with conditions such as Lumbar disc herniation, severe scoliosis, or neurological disorders that may interfere with the study s outcomes. Recent Surgery or Injury: Participants who have undergone surgery or experienced significant injury to the Back, or Hip within the last 6 months. Current Participation in Physical Therapy: Individuals currently receiving physical therapy or other interventions for LCS or related conditions. Contraindications to PNF: Includes participants with medical conditions or physical limitations that would contraindicate the use of PNF techniques, such as severe osteoporosis or acute inflammatory conditions. Pregnancy: Pregnant individuals are excluded due to potential variability in physical condition and the effects of pregnancy on posture and musculoskeletal health. Non-Compliance: Individuals who are unable or unwilling to comply with the study protocol, including attending scheduled sessions and following prescribed exercises.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain Levels: Measurement Tool: Numeric Rating Scale (NRS). Description: A subjective measure where participants rate their pain on a scale from 0 (no pain) to 10 (worst possible pain). Muscle Strength: Measurement Tool: Manual Muscle Testing (MMT). Description: Evaluation of the strength of key muscle groups involved in Lower Cross Syndrome, including deep hip flexors, Gluteus maximus. Timepoint: 1st and 2nd week | — |
Secondary
| Measure | Time frame |
|---|---|
| Functional Capacity: Measurement Tool: Functional Movement Screen (FMS) Description: Assessment of the participant s ability to perform specific functional movements and tasks related to their work or daily activities, focusing on movements impacted by LCS. Quality of Life: Measurement Tool: Short Form Health Survey (SF-36) Description: A broad assessment of the participant s overall quality of life, including physical, emotional, and social functioning, with a focus on how LCS impacts daily living.Timepoint: 1st and last week of treatment | — |
Countries
India
Contacts
Public ContactSachin Kumar
GALGOTIAS UNIVERSITY
Outcome results
None listed