Health Condition 1: M999- Biomechanical lesion, unspecified
Conditions
Interventions
Intervention1: Transdermal Magnesium Spray: Participants in the intervention group will receive hot fomentation for 10 minutes followed by isotonic neck exercises using theraband 3 sets twice daily. I
Sponsors
Galgotias University
Eligibility
Inclusion criteria
Inclusion criteria: 1. Persistent Neck Pain duration more than 3 months. 2. Health Status: Individuals without diagnosed medical conditions affecting magnesium metabolism or utilization. 3. Ability to Provide Informed Consent: Participants must be capable of understanding the study procedures and providing informed consent. 4. Availability: Participants must be available for the duration of the study and willing to adhere to the intervention protocol.
Exclusion criteria
Exclusion criteria: 1. Known Magnesium Deficiency: Individuals with diagnosed magnesium deficiency or receiving magnesium supplementation at the time of enrollment. 2. Chronic Medical Conditions: Participants with chronic medical conditions (e.g., renal disease, gastrointestinal disorders) known to affect magnesium absorption or metabolism. 3. Medication Use: Individuals currently taking medications known to interfere with magnesium absorption or metabolism (e.g., proton pump inhibitors, diuretics). 4. Pregnancy or Lactation: Pregnant or lactating individuals, as magnesium requirements may differ during these periods. 5. Allergy or Sensitivity: Individuals with known allergies or sensitivities to magnesium or any components of the supplementation product (e.g., Spray 10 spray). 6. Participation in Other Clinical Trials: Participants currently enrolled in or have participated in other clinical trials within a specified timeframe prior to enrollment. 7. Inability to Comply: Individuals unable or unwilling to adhere to the study protocol, including attending scheduled assessments and following supplementation instructions.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pressure pain threshold using Algometer The Petersberg Sleep Quality Index Patient Global Perception of Change questionnaireTimepoint: Baseline, 6 weeks and 12 weeks | — |
Secondary
| Measure | Time frame |
|---|---|
| Neck Disability Index will be used to assess the degree of disability & limitations experienced by individuals suffering from neck pain. Timepoint: Baseline, 6 weeks & 12 weeks | — |
Countries
India
Contacts
Public ContactDr Aksh Chahal
Galgotias University
Outcome results
None listed