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Comparative Effects of Dry Needling and Cross Friction Massage on Patients With Plantar Fascitis, RCT

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT05915091
Recruitment Status : Active, not recruiting
First Posted : June 22, 2023
Last Update Posted : June 22, 2023
Sponsor:
Information provided by (Responsible Party):
Muhammad Naveed Babur, Superior University

Tracking Information
First Submitted Date  ICMJE June 13, 2023
First Posted Date  ICMJE June 22, 2023
Last Update Posted Date June 22, 2023
Actual Study Start Date  ICMJE April 1, 2023
Actual Primary Completion Date June 1, 2023   (Final data collection date for primary outcome measure)
Current Primary Outcome Measures  ICMJE
 (submitted: June 13, 2023)
  • Pain Scale of Plantar Fasciitis [ Time Frame: 3 Months ]
  • Foot Health Status Questioner Score [ Time Frame: 3 Months ]
  • Foot Function Index Score [ Time Frame: 3 Months ]
Original Primary Outcome Measures  ICMJE Same as current
Change History No Changes Posted
Current Secondary Outcome Measures  ICMJE Not Provided
Original Secondary Outcome Measures  ICMJE Not Provided
Current Other Pre-specified Outcome Measures Not Provided
Original Other Pre-specified Outcome Measures Not Provided
 
Descriptive Information
Brief Title  ICMJE Comparative Effects of Dry Needling and Cross Friction Massage on Patients With Plantar Fascitis, RCT
Official Title  ICMJE Comparative Effects of Dry Needling and Cross Friction Massage on Patients With Plantar Fascitis, a Randomized Controlled Trial
Brief Summary Effectiveness Comparative Effects of Dry Needling and Cross Friction Massage on Patients With Plantar Fascitis
Detailed Description Not Provided
Study Type  ICMJE Interventional
Study Phase  ICMJE Not Applicable
Study Design  ICMJE Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Health Services Research
Condition  ICMJE Plantar Fascitis
Intervention  ICMJE
  • Diagnostic Test: Dry Needling
    Dry needling is a treatment that healthcare providers use for pain and movement issues associated with myofascial trigger points. With this technique, a provider inserts thin needles into or near your trigger points. The needles stimulate your muscles, which causes them to contract or twitch
  • Other: Cross Friction Massage
    Cross friction massage breaks down scar tissue and remodels the tissue into more flexible, pliable, and functional, healthy soft tissue. Also known as transverse friction massage, this technique is a deep tissue massage technique performed at the site of injury
Study Arms  ICMJE
  • Experimental: Dry Needling
    Intervention: Diagnostic Test: Dry Needling
  • Cross Friction Massage
    Intervention: Other: Cross Friction Massage
Publications * Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment Status  ICMJE Active, not recruiting
Actual Enrollment  ICMJE
 (submitted: June 13, 2023)		 60
Original Actual Enrollment  ICMJE Same as current
Estimated Study Completion Date  ICMJE August 31, 2023
Actual Primary Completion Date June 1, 2023   (Final data collection date for primary outcome measure)
Eligibility Criteria  ICMJE

Inclusion Criteria:

  • Patients With Plantar Fascitis

Exclusion Criteria:

  • Other Health Issues
Sex/Gender  ICMJE
Sexes Eligible for Study: All
Ages  ICMJE 35 Years to 40 Years   (Adult)
Accepts Healthy Volunteers  ICMJE No
Contacts  ICMJE Contact information is only displayed when the study is recruiting subjects
Listed Location Countries  ICMJE Pakistan
Removed Location Countries  
 
Administrative Information
NCT Number  ICMJE NCT05915091
Other Study ID Numbers  ICMJE DPT/Batch-Fall18/544
Has Data Monitoring Committee Yes
U.S. FDA-regulated Product
Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
IPD Sharing Statement  ICMJE Not Provided
Current Responsible Party Muhammad Naveed Babur, Superior University
Original Responsible Party Same as current
Current Study Sponsor  ICMJE Superior University
Original Study Sponsor  ICMJE Same as current
Collaborators  ICMJE Not Provided
Investigators  ICMJE Not Provided
PRS Account Superior University
Verification Date June 2023

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP