- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05969769
Effect of Thoracic Mobilization in Females With Coccydynia
August 18, 2023 updated by: Riphah International University
Effects of Thoracic Manual Mobilization Techniques in Females of Coccydynia
Coccydynia is common and prevalent among the females and several types of exercises and electrotherapy are advised.
Pain can reduced significantly with both short wave diathermy and muscles stretches.
There is limited evidence on indirect method like thoracic mobilization techniques to improve coccydynia.
This study will determine the effects of thoracic mobilization techniques on coccydynia.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
Coccydynia, refers to pain in the coccyx region.
it can be caused by various factor including trauma or injury (such as falls or child birth ), repetitive strain, prolong sitting on hard surface, or even idiopathic reasons.
Treatment options for Coccydynia may include conservative measures, such as pain medication, using cushion or donut-shaped pillows to relieve pressure, applying heat or cold packs, and avoiding activities that's exacerbate the pain.
Physical therapy including exercises such as stretching, Muscle Energy Technique (MET) can also be beneficial in some cases.
Thoracic manual therapy, which involves hands-on techniques applied to the thoracic spine, can indeed be beneficial for improving spine mobility.
While it may not directly target the coccyx itself, improving overall spinal mobility can have indirect effects on coccyx pain and dysfunction.
Study Type
Interventional
Enrollment (Estimated)
44
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Imran Amjad, PhD
- Phone Number: 03324390125
- Email: Imran.amjad@riphah.edu.pk
Study Locations
-
-
KPK
-
Peshawar, KPK, Pakistan
- Recruiting
- Rahman Medical Hospital
-
Contact:
- Summra Andleeb, MS(0MPT)
- Phone Number: 03450617872
- Email: sammra.andleeb@riphah.edu.pk
-
Sub-Investigator:
- Laiba Zahid, MS(WHPT)
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Diagnosed females coccydynia patients.
Exclusion Criteria:
- Pregnancy
- 6 Months past Surgery, fracture or dislocation of coccyx.
- Malignancy or cyst in the pelvic area.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Experimental Group
Sustained Natural Apophyseal Glides will be performed with Muscle Energy Technique and Short Wave Diathermy as experimental group.
|
Sustained Natural Apophyseal Glides 3 sets of 10 reps with 1 min rest btw sets.
|
|
Active Comparator: Control Group
Short wave diathermy will be given with Muscle Energy Techniques.
|
Short wave diathermy for 10 to 15 mins Muscle Energy Techniques of following muscles will be performed, Hip flexors muscles, Quadrates lamborum muscles, Erector spinae muscles, Piriformis muscles, PFS technique of METs Isometric hold 5-7 sec, Stretching 15 sec, Rest 30 sec.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Modified OSWESTRY Low Back pain Index
Time Frame: 8th Week
|
Changes from the baseline ODI is a disease specific disability measure is used to establish a level of disability stage on a patient activity status and monitor change over the time.
The ODI is made up of 10 questions.
Each question is scored from (o-5) m
|
8th Week
|
|
Numeric Pain Rating Scale
Time Frame: 8th Week
|
Changes from the baseline Numeric Pain Rating Scale will be used to assess pain.
• The Numeric Pain Rating Scale is an eleven-point measure of pain: the patient rates pain from 0 (no pain) to 10 (worst imaginable pain).
The NPRS has shown good responsiveness in shoulder pain.
|
8th Week
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: summra andleeb, MS(OMPT), riphah internation university
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
August 1, 2023
Primary Completion (Estimated)
January 1, 2024
Study Completion (Estimated)
February 1, 2024
Study Registration Dates
First Submitted
July 23, 2023
First Submitted That Met QC Criteria
July 23, 2023
First Posted (Actual)
August 1, 2023
Study Record Updates
Last Update Posted (Actual)
August 22, 2023
Last Update Submitted That Met QC Criteria
August 18, 2023
Last Verified
August 1, 2023
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- Laiba Zahid
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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