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Effect of Neurogenic Acupoint CUPPING ON WOMEN WITH CHRONIC PELVIC PAIN

Primary Purpose

Chronic Pelvic Pain

Status
Unknown status
Phase
Not Applicable
Locations
Egypt
Study Type
Interventional
Intervention
dry cupping
Life style modification
Sponsored by
Ministry of Health and Population, Egypt
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Pelvic Pain focused on measuring chronic pelvic pain, dry cupping, neurogenic acupoint

Eligibility Criteria

25 Years - 40 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • thirty married women suffering from chronic pelvic pain
  • Their age will range from 25 to 40 years old.
  • Their BMI will be ≤ 30 kg/m2.
  • They should be non-smokers.
  • They should have sedentary life style without participation at any exercise training program during this study.
  • Maximum parity number is three.
  • Their score is less than 6 on The Interstitial Cystitis Symptom Index and Problem Index" (The O'Leary-Sant), to exclude Interstitial Cystitis.
  • Their score on visual analog scale above 5.
  • Their muscle strength is good in hip abductor, adductor, external rotator and internal rotator muscles .
  • Their pelvic floor muscle strength is good.

Exclusion Criteria:

  • Women having any serious physical disorders such as vertebral fractures, disk hernia, acute inflammation and deep venous thrombosis.
  • Women having any problems in the acupoints such as fractures, ulcers, varicose veins, skin disease or inflammation.
  • Women having history of cancer or congenital anomaly.
  • Use of any kind of analgesic medications or contraceptive pills.
  • Diabetic or hypertensive patient.
  • Have any auto immune disease (rheumatoid, lupus), chest disease and cardiac disease.
  • HS-CRP test exclusion patient during menses, patient suffering any medical condition increase inflammation ex cough, sneezing.
  • Patient suffering from chronic pelvic pain due to another cause except PID.

Sites / Locations

  • They will be selected from 6th District Family Medicine Unit, Giza.Recruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

dry cupping

Life style modification

Arm Description

Dry cupping is considered to be a noninvasive and inexpensive technique, used worldwide to treating patients with pain syndromes It is in fact a type of physical therapy which is applied by the specialists of acupuncture or other individuals. It improves the subcutaneous blood flow and, as a result, stimulates the autonomic nervous system and reduces the pai

lifestyle modifications in the form of dietary recommendations, exercises and sleep quality improvement for 8 weeks.The life style modification followed in the treatment: Avoid consumption of all kinds of alcohol beverages. Avoid consumption of spicy foods, pepper, chili and coffee Follow a correct diet assuming each day 50% carbohydrates,30% fats and 20% proteins Increase your intake of fruits, vegetables and foods rich of natural fibers (dark bred, vegetables, spinaches). 8 hour sleep at night 40 minutes of walking 3time per week.

Outcomes

Primary Outcome Measures

High sensitive C - reactive protein (Hs-CRP)
Short-Form McGill Pain Questionnaire (SF-MPQ)
It is a reliable and valid instrument that is easier and quicker to use in clinical research than the McGill pain questionnaire (MPQ). It will be used to evaluate pain intensity for each woman in both groups before and after the end of treatment program. It consists of 15 descriptors (11 sensory; 4 affective) which are rated on an intensity scale as 0 = none, 1 = mild, 2 = moderate or 3 = severe.
Pelvic Pain Impact Questionnaire (PPIQ)
a questionnaire that assesses the impact of pelvic pain on women, that has high utility, sound psychometric performance, easy scoring, and high reliability, 10-item questionnaire consisted of 8 Likert questions and 2 supplemental, nonscored questions, the questionnaire targeted the pelvic pain population well, had appropriate Likert categories, constituted a unidimensional scale, and showed internal consistency. Test-retest reliability was highPelvic Pain Impact Questionnaire assesses the life impact of pelvic pain. It uses patient-generated language, is easily administered and scored, has very strong psychometric properties, and it is suitable for research and clinical settings across primary, secondary, and tertiary care

Secondary Outcome Measures

Full Information

First Posted
June 2, 2020
Last Updated
June 16, 2020
Sponsor
Ministry of Health and Population, Egypt
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1. Study Identification

Unique Protocol Identification Number
NCT04436445
Brief Title
Effect of Neurogenic Acupoint CUPPING ON WOMEN WITH CHRONIC PELVIC PAIN
Official Title
Effect of Neurogenic Acupoint Cupping on Hs-CRP and Pain Perception in Women With Chronic Pevic Pain
Study Type
Interventional

2. Study Status

Record Verification Date
June 2020
Overall Recruitment Status
Unknown status
Study Start Date
July 15, 2018 (Actual)
Primary Completion Date
September 1, 2020 (Anticipated)
Study Completion Date
September 1, 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ministry of Health and Population, Egypt

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
PURPOSE: The purpose of this study is to determine the effect of dry cupping on women with chronic pelvic pain. BACKGROUND: Recent studies have examined the efficacy of dry cupping on acupoints for various pain-related conditions. They showed good result . However, no studies up to date has been evaluated the effect of dry cupping in treating Chronic pelvic pain. Therefore, this study is the first one which aims to investigate the effect of dry cupping on women suffering from Chronic pelvic pain. This study may expand the role of physiotherapy in woman's health. HYPOTHESE: There is no effect of bioptron light therapy on postmenopausal osteoporosis. RESEARCH QUESTION: There is no effect of dry cupping on chronic pelvic pain.
Detailed Description
Chronic pelvic pain is a highly prevalent debilitating disease with negative impact on the quality of life and productivity of women. The estimated prevalence of CPP is 3.8% among women aged 15-73 years, ranging from 14% to 24% among women of reproductive age, with a direct impact on their marital, social and professional life . A specific diagnosis for CPP is often difficult; no diagnosis is made in 60% of patients . Treatment of these patients remains a challenge due to the diverse clinical signs and phenotypes. Several non-surgical as well as surgical strategies exist. However, many of the therapy approaches seem to have only limited effect in managing CPP . Additionally, many of the recommended medical and surgical interventions have a potential for harm in a proportion of women . Accordingly, an alternative therapeutic approach is desirable. Dry cupping is considered to be a noninvasive and inexpensive technique, used worldwide to treating patients with pain syndromes . It is in fact a type of physical therapy which is applied by the specialists of acupuncture or other individuals. It improves the subcutaneous blood flow and, as a result, stimulates the autonomic nervous system and reduces the pain . The application of suction on selected acupoints produces hyperemia or hemostasis, which may result in a therapeutic effect .When compared to acupuncture, cupping therapy is a non-invasive therapy with relatively shorter treatment duration and less treatment cost . Recent studies have examined the efficacy of dry cupping on acupoints for various pain-related conditions. They showed good results . However, no studies up to date has been evaluated the effect of dry cupping in treating CPP. Therefore, this study is the first one which aims to investigate the effect of dry cupping on women suffering from CPP. This study may expand the role of physiotherapy in woman's health

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Pelvic Pain
Keywords
chronic pelvic pain, dry cupping, neurogenic acupoint

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
women's with chronic pelvic pain
Masking
Investigator
Allocation
Randomized
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
dry cupping
Arm Type
Active Comparator
Arm Description
Dry cupping is considered to be a noninvasive and inexpensive technique, used worldwide to treating patients with pain syndromes It is in fact a type of physical therapy which is applied by the specialists of acupuncture or other individuals. It improves the subcutaneous blood flow and, as a result, stimulates the autonomic nervous system and reduces the pai
Arm Title
Life style modification
Arm Type
Active Comparator
Arm Description
lifestyle modifications in the form of dietary recommendations, exercises and sleep quality improvement for 8 weeks.The life style modification followed in the treatment: Avoid consumption of all kinds of alcohol beverages. Avoid consumption of spicy foods, pepper, chili and coffee Follow a correct diet assuming each day 50% carbohydrates,30% fats and 20% proteins Increase your intake of fruits, vegetables and foods rich of natural fibers (dark bred, vegetables, spinaches). 8 hour sleep at night 40 minutes of walking 3time per week.
Intervention Type
Combination Product
Intervention Name(s)
dry cupping
Intervention Description
represents the location and clinical importance of each acupoint. First, the position of the patient will be supine lying for SP6, SP9, KI6, GB34 and CV6 acupoints and it will be prone lying for B23 acupoint. Second, the skin will be cleaned by alcohol then cups will be placed on the acupoints. Dry cupping for SP6, SP9, KI6 and GB34 acupoints will be applied using small cups while dry cupping for CV6 and B23 will be applied using large cups. Third, a negative pressure will be applied with a manual handle. Finally, the cups will be removed after 5 to 15 minutes by pressing one side of the skin with a finger to release the vacuum slowly.
Intervention Type
Other
Intervention Name(s)
Life style modification
Intervention Description
Life style modification
Primary Outcome Measure Information:
Title
High sensitive C - reactive protein (Hs-CRP)
Time Frame
8 weeks
Title
Short-Form McGill Pain Questionnaire (SF-MPQ)
Description
It is a reliable and valid instrument that is easier and quicker to use in clinical research than the McGill pain questionnaire (MPQ). It will be used to evaluate pain intensity for each woman in both groups before and after the end of treatment program. It consists of 15 descriptors (11 sensory; 4 affective) which are rated on an intensity scale as 0 = none, 1 = mild, 2 = moderate or 3 = severe.
Time Frame
8 weeks
Title
Pelvic Pain Impact Questionnaire (PPIQ)
Description
a questionnaire that assesses the impact of pelvic pain on women, that has high utility, sound psychometric performance, easy scoring, and high reliability, 10-item questionnaire consisted of 8 Likert questions and 2 supplemental, nonscored questions, the questionnaire targeted the pelvic pain population well, had appropriate Likert categories, constituted a unidimensional scale, and showed internal consistency. Test-retest reliability was highPelvic Pain Impact Questionnaire assesses the life impact of pelvic pain. It uses patient-generated language, is easily administered and scored, has very strong psychometric properties, and it is suitable for research and clinical settings across primary, secondary, and tertiary care
Time Frame
8 weeks

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
25 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: thirty married women suffering from chronic pelvic pain Their age will range from 25 to 40 years old. Their BMI will be ≤ 30 kg/m2. They should be non-smokers. They should have sedentary life style without participation at any exercise training program during this study. Maximum parity number is three. Their score is less than 6 on The Interstitial Cystitis Symptom Index and Problem Index" (The O'Leary-Sant), to exclude Interstitial Cystitis. Their score on visual analog scale above 5. Their muscle strength is good in hip abductor, adductor, external rotator and internal rotator muscles . Their pelvic floor muscle strength is good. Exclusion Criteria: Women having any serious physical disorders such as vertebral fractures, disk hernia, acute inflammation and deep venous thrombosis. Women having any problems in the acupoints such as fractures, ulcers, varicose veins, skin disease or inflammation. Women having history of cancer or congenital anomaly. Use of any kind of analgesic medications or contraceptive pills. Diabetic or hypertensive patient. Have any auto immune disease (rheumatoid, lupus), chest disease and cardiac disease. HS-CRP test exclusion patient during menses, patient suffering any medical condition increase inflammation ex cough, sneezing. Patient suffering from chronic pelvic pain due to another cause except PID.
Facility Information:
Facility Name
They will be selected from 6th District Family Medicine Unit, Giza.
City
Giza
ZIP/Postal Code
00202
Country
Egypt
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
rehab tareq tareq mohamad
Phone
00201111287279
Email
rehabtareqmohamad@gmail.com

12. IPD Sharing Statement

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Effect of Neurogenic Acupoint CUPPING ON WOMEN WITH CHRONIC PELVIC PAIN

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