Comparing two treatments for tailbone pain
Comparative Effects of Levator Ani Release and Post Isometric Relaxation on Pain, Disability, and Quality of Life Among Patients With Coccydynia
This study is testing whether two different treatment methods can help people with tailbone pain feel better and improve their daily life.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 46 (estimated) |
| Ages | 20 Years to 40 Years |
| Sex | All |
| Sponsor | Riphah International University Academic / other |
| Locations | 1 site (Lahore, Punjab) |
| Trial ID | NCT06109077 on ClinicalTrials.gov |
What this trial studies
This study aims to compare the effects of levator ani release exercises and post isometric relaxation techniques on pain, disability, and quality of life in patients suffering from coccydynia. A randomized control trial will be conducted at Jinnah Hospital in Lahore, involving 46 participants who will be randomly assigned to one of two treatment groups. The effectiveness of each intervention will be assessed using a pain and disability questionnaire at the start and after four weeks of treatment. Data analysis will be performed using SPSS software to determine the outcomes of each treatment method.
Who should consider this trial
Good fit: Ideal candidates for this study are individuals aged 20-40 years who are drivers, office workers, or computer users experiencing tailbone pain.
Not a fit: Patients with neurological disorders, bone deficits, vascular abnormalities, rheumatoid arthritis, ankylosing spondylitis, fractures, or tumors may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide effective non-surgical treatment options for patients suffering from coccydynia.
How similar studies have performed: While there is limited data on the specific interventions being compared, similar studies have shown promise in treating coccydynia with physical therapy techniques.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria:• * Both gender * Age between 20-40 years * Drivers * Office workers * Computer users * Both gender * Age between 20-40 years * Drivers * Office workers * Computer users Exclusion Criteria: * Neurological disorders, * Bone deficits, * Vascular abnormalities, * Rheumatoid arthritis * Ankylosing spondylitis * Fracture * Tumor
Where this trial is running
Lahore, Punjab
- Ittefaq — Lahore, Punjab, Pakistan (Recruiting)
Study contacts
- Principal investigator: Humera Mubashar, Ms — Riphah International University
- Study coordinator: Imran Amjad, Phd
- Email: imran.amjad@riphah.edu.pk
- Phone: 03324390125
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.