Effects of Lateral Femoral Cutaneous Nerve Mobilization With and Without Muscle Energy Techniques in Pregnant Females
1 other identifier
interventional
48
1 country
2
Brief Summary
The rationale of this study is to provide empirical evidence regarding the efficacy and safety of neural mobilization in pregnant women with meralgia paresthetica. By investigating the potential benefits of this intervention, healthcare professionals can make informed decisions about incorporating neural mobilization into the management of this condition during pregnancy. Focusing on the impact of neural mobilization and muscle energy techniques on both neuropathic pain and quality of life aligns with a patient-centered approach to care. The goal is not only to reduce symptoms but also to enhance overall well-being and functional capacity
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Dec 2024
Shorter than P25 for not_applicable
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
December 20, 2024
CompletedStudy Start
First participant enrolled
December 23, 2024
CompletedFirst Posted
Study publicly available on registry
December 27, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 15, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
May 15, 2025
CompletedJuly 25, 2025
July 1, 2025
5 months
December 20, 2024
July 21, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
quality of life is assessed by QOL questioner
EQ-5D is used to measure quality of life
at base line pre intervention, at the end of 4th week post intervention
Knee range of motion is used to measure ROM
measured by goniometer
at base line pre intervention, at the end of 4th week post intervention
neuropathic pain
The Neuropathic Pain Scale (NPS) is a tool used to assess the specific qualities of pain associated with neuropathic pain. It helps differentiate neuropathic pain from other types of pain by evaluating different pain sensations and their intensity. The NPS consists of 10 items, each rated on a scale of 0 to 10, where 0 is "no pain" and 10 is the "worst imaginable pain".
at base line pre intervention, at the end of 4th week post intervention
Study Arms (2)
group A
EXPERIMENTALLateral Femoral cutaneous nerve mobilization with muscle energy techniques
GROUP B
EXPERIMENTALInterventions
It consists of 24 patients who were assessed by prone knee bend (PKB) test and knee range of motion was measured by goniometer. In addition to traditional physical therapy and muscle energy procedures, patients in this group received neural mobilization. The patient laid on their side with their knee bent to a 90-degree angle and the affected side looking up while neural mobilization was carried out. The therapist then performed the technique by abducting and extending the patient's hip. Five repetitions of the nerve stretch were performed, each with a 10-second hold and a 5-second rest in between. METs were implemented in two positions using post-isometric relaxation (PIR): In this initial posture, the patient laid on their back with the affected leg just over the bed's edge. With one hand, the physiotherapist stood facing the affected side and pressed the contralateral ASIS to keep the patient from rolling off the bed. The therapist, however, simultaneously grabbed the femur dist
It involves 24 patients who had received the neural mobilization described above along with traditional physical therapy that does not involve muscular energy techniques. The treatment took place in the outpatient physical therapy department and lasted around thirty minutes in total
Eligibility Criteria
You may qualify if:
- Age ranges from 18 to 40 years
- Body mass index ≥25kg/m2.
- Pregnant females in third trimester diagnosed with myalgia paraesthetica.
- Multigravida pregnant females
- Patients will be screened through Prone Knee Bend (PKB) test for femoral nerve compression.
- Positive pelvic compression test(1)
You may not qualify if:
- Those having other entrapment syndromes or radicular symptoms
- Motor weakness
- Having a history or ongoing cancerous proliferation
- Active infection
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (2)
Ghurkhi Hospital
Lahore, Punjab Province, Pakistan
Ghurki Hospital
Lahore, Punjab Province, Pakistan
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Iqra abdul ghafoor, PPDPT
Riphah International University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Masking Details
- outcome assessor was kept blinded
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 20, 2024
First Posted
December 27, 2024
Study Start
December 23, 2024
Primary Completion
May 15, 2025
Study Completion
May 15, 2025
Last Updated
July 25, 2025
Record last verified: 2025-07
Data Sharing
- IPD Sharing
- Will not share