- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07605299
"Comparative Effect of Rolfing Soft Tissue Manipulation and Bowen Technique on Calf Tightness Among Housewives"
May 22, 2026 updated by: Ayesha Zulfiqar, Rashid Latif Medical College
Comparative effect of Rolfing Soft Tissue Manipulation and Bowen Technique on calf tightness among housewives.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Housework involves ongoing physical effort and is predominantly carried out by women.
As a result, musculoskeletal (MSK) problems in housewives are a significant concern.
Tightness in the calf muscles can limit ankle dorsiflexion, contributing to such issues.
Two potential manual therapy interventions, Rolfing Soft Tissue Manipulation (RSTM) and the Bowen Technique (BT) may help alleviate this condition.
Study Type
Interventional
Enrollment (Actual)
54
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 Locations
-
-
Punjab Province
-
Lahore, Punjab Province, Pakistan, 54000
- Arif Memorial Teaching Hospital
-
-
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:
Housewives of age 25-50 years
- Limited ankle dorsiflexion range of motion <10∘ of ankle dorsiflexion
- Calf muscle tightness on palpation
Exclusion Criteria:
A history of foot and ankle surgery
- Neurological symptoms indicating a prolapsed intervertebral disc or radiating pain and comorbidities.
- Any previous Neuromuscular issue, lower extremity pain and any pathology, toe Walkers, pregnant females, fracture of lower extremity and congenital deformity of lower extremity were excluded
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 |
|---|---|
|
Experimental: Rolfing Soft Tissue Manipulation
Rolfing soft tissue manipulation aimed to separate bound up fascia by deeply separating the fibers manually to loosen them and allow efficient movement patterns.
Rolfing practitioners use their hands, knuckles, elbows and more to "release, realign and balance the whole body".
The fascia manipulated until it can operate in conjunction to the muscles in a normal fashion
|
The initial intervention involved applying a hot pack to the calf muscles (10-minute duration), then with the participant in the prone position and the therapist by their side, a 120-second hold of the Rolfing technique of MFR was applied for the calf muscle
|
|
Active Comparator: Bowen Technique
Bowen technique is described as a soft tissue remedial therapy, the therapist uses fingers or thumbs to apply pain-free, gentle rolling moves over muscle, ligament, tendon and other connective tissues in specific parts of the body
|
The Bowen Technique involves the application of gentle rolling motions on specific target muscles or connective tissues using the fingers and thumbs, typically ranging from fifteen to forty-five minutes per session,
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Goniometer
Time Frame: Baseline and 4th week
|
Goniometer is easily accessible and is an important tool for measuring range of motion of different joints.
To measure DFROM using a goniometer, participants were instructed to lay supine and with the knee straight and actively dorsiflex their ankles to end of range by bringing their toes up towards their head.
For angle measurement, the axis center of the goniometer was placed on the most prominent point of the lateral malleolus, with the fixed arm of the goniometer along with the leg, and the movable arm parallel with the sole of the foot
|
Baseline and 4th week
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
WBLT (knee to wall test)
Time Frame: Baseline and 4th week
|
A tape measure was used.
|
Baseline and 4th week
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Lee K, Lewis GN. Short term relief of multisite chronicpain with Bowen Therapy: A double-blind, randomized controlled trial. J Bodyw Mov Ther. 2020 Oct;24(4):271-279. doi: 10.1016/j.jbmt.2020.06.025. Epub 2020 Jul 30.
- KALIYAPERUMAL, A., DHARANI, J. & NEELAMEGAM, D. 2021. Comparison between indian and western toilet user on hamstring and ankle flexibility among housewives. International Journal of Physical Education Sports Management and Yogic Sciences, 11, 13-22.
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)
July 10, 2024
Primary Completion (Actual)
January 12, 2025
Study Completion (Actual)
January 12, 2025
Study Registration Dates
First Submitted
May 18, 2026
First Submitted That Met QC Criteria
May 18, 2026
First Posted (Actual)
May 22, 2026
Study Record Updates
Last Update Posted (Actual)
May 27, 2026
Last Update Submitted That Met QC Criteria
May 22, 2026
Last Verified
May 1, 2026
More Information
Terms related to this study
Other Study ID Numbers
- IRB/2024/158
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
The data will be shared on request.
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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