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Effect of Acupressure on Carpal Tunnel Syndrome in Pregnant Women

Effect of Acupressure on Carpal Tunnel Syndrome in Pregnant Women

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06555926
Enrollment
50
Registered
2024-08-15
Start date
2024-08-31
Completion date
2024-12-31
Last updated
2024-08-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Carpal Tunnel Syndrome

Brief summary

This study will be conducted to investigate the effect of acupressure on carpal tunnel syndrome in pregnant women.

Detailed description

The pregnant women are more prone to develop carpal tunnel syndrome because they retain more fluid during the later stages of their pregnancies. The more fluid retained , the more swelling occurs , squeezing the nerves that run through the hand and finger. Also most women who experience pain, numbness and tingling in the hand for the first time due to pregnancy have no idea that they have carpal tunnel syndrome. Given the importance of treating CTS and preventing the limitations caused by this syndrome, and since it can turn into a debilitating disease if left untreated, acupressure can be recommended as a safe and noninvasive technique for reducing the severity of clinical symptoms. Till now, there is no previous studies explored the effect of acupressure on carpal tunnel syndrome in pregnant women. So, this study will be conducted to provide new information about the efficacy of acupressure in management of carpal tunnel syndrome in pregnant women, which will help such pregnant women to overcome this problem and will add new evidence to the field of physical therapy.

Interventions

OTHERAcupressure

The pregnant women will receive acupressure on the (Pc-6/Lung-7 )acupoints one minute for each point with 3 repetitions on both side( about 30minutes /session),2 times per week in addition to advices for 12 weeks.

OTHERadvices for relieving carpal tunnel syndrome

The pregnant women will receive advices for 12 weeks as follows: * Avoid heavy lifting. * Avoid repetitive tasks. * Sit on chairs with armrests and elevate affected hand on the armrest * Avoid sleeping on the side of the affected hand. * Keep the wrist in a neutral (straight) position. * Avoid positions of full flexion and extension. * Reduce general swelling by: * eating less salty food . * elevating legs when sitting . * wearing compression garments. * Apply cold water over the wrist.

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

* Pregnant women who are clinically diagnosed as having carpal tunnel syndrome . * Their age will be ranged from 20 to 35years old. * Their body mass index will not exceed 30kg/m2. * All of them are in their 3rd trimester of pregnancy.(28-40weeks) * All of them suffer from mild and moderate CTS. * Degree of carpal tunnel pain will be 2 or more on Visual Analogue scale.

Exclusion criteria

* Dermatological abnormalities in the skin of acupionts. * Internal fixation at the area of acupressure application. * Smokers . * Metabolic diseases such as Diabetes mellitus. * Females who had history of fracture or trauma to the hand .

Design outcomes

Primary

MeasureTime frameDescription
Assessment of pain severity12 weeksThe pain intensity will be assessed for all participants in both groups before and after treatment through VAS. It is a 10 cm horizontal line on which the participant's pain intensity will be represented by a point between the extremes of no pain at all and worst imaginable pain. Each participant will be asked to mark a point on a VAS line between the extremes that related to her current pain intensity
median nerve conduction study12 weeksComputerized Electromyography (Dantce): ATOENINIES neuro screen system will be used to perform median nerve conduction study before and after the treatment program for all participants in both groups

Contacts

Primary Contactbassant ahmed, Master
besobassant88@gmail.com+201141292300
Backup Contactmohamed fawzy, PHD
drmohamedfawzy61@icloud.com+201001414404

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026