NCT07482371 Comparative Effects of Scooping Mobilization and Dynamic Cupping Therapy on Elbow Stiffness
| NCT ID | NCT07482371 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Riphah International University |
| Condition | Children |
| Study Type | INTERVENTIONAL |
| Enrollment | 28 participants |
| Start Date | 2025-10-22 |
| Primary Completion | 2026-06-02 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 28 participants in total. It began in 2025-10-22 with a primary completion date of 2026-06-02.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
The current study is a randomized clinical trial, data is collected from Alqamar Hospital Shakarghar. The study includes 28 patients equally divided into two groups and randomly allocated. Inclusion criteria for the study will be children of age group 6-13, children with diagonosis of post fracture stiff elbow minimal immobilized period of 3 weeks. Patients with any neurological impairment, children with MSK disorders, Infection or tumors will be excluded from the study. Experimental Scooping mobilization group will receive scooping mobilization combined with electrotherapy for 2 minutes per session 5 days a week. Experimental dynamic cupping group will receive dynamic cupping therapy combined with electrotherapy for 10 minutes per session 5 days a week. Total intervention period will be of 4 weeks. Data collection will be done before and after the intervention. Tools used for data collection will be Goniometer and Quick DASH Questionnaire. Data will be analyzed through SPSS version 27.00.
Eligibility Criteria
Inclusion Criteria: * Children of age group 6-13 * Children with diagnosis of post-fracture elbow stiffness. * Minimal immobilized period of 3 weeks * Children with age group of both genders Exclusion Criteria: * Infection or tumers * Neurological impairment * Children with MSK disorders * Metabolic bone disease * Pathological fractures
Contact & Investigator
Adil Munir, MSPT
PRINCIPAL INVESTIGATOR
Riphah International University
Frequently Asked Questions
Who can join the NCT07482371 clinical trial?
This trial is open to participants of all sexes, aged 6 Years or older, up to 13 Years, studying Children. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07482371 currently recruiting?
Yes, NCT07482371 is actively recruiting participants. Contact the research team at imran.amjad@riphah.edu.pk for enrollment information.
Where is the NCT07482371 trial being conducted?
This trial is being conducted at Lahore, Pakistan.
Who is sponsoring the NCT07482371 clinical trial?
NCT07482371 is sponsored by Riphah International University. The principal investigator is Adil Munir, MSPT at Riphah International University. The trial plans to enroll 28 participants.