Use of TENS Unit in the Management of Endometriosis Pain
Primary Purpose
Endometriosis, Pelvic Pain
Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Ovira Transcutaneous Electrical Nerve Stimulation Unit
Sponsored by
About this trial
This is an interventional supportive care trial for Endometriosis
Eligibility Criteria
Inclusion Criteria:
- Females ages 18-45 years at time of enrollment
- A surgical diagnosis with direct visualization and/or histopathologic confirmation of endometriosis
- Average monthly endometriosis pain flare
- Naïve TENS user
Exclusion Criteria:
TENS device exclusion:
- Implantable devices (pacemaker, Interstim, etc.)
- Cardiac arrhythmia
- Open skin sores over areas of placement
- Pregnancy
- Nursing or trying to conceive at this time
- Post-operative <12 weeks from abdominal or pelvic surgery
- Planned surgery or hormonal medication changes for duration of study if applicable
- Non-English speaking or inability to read and understand English
- Prisoners
Sites / Locations
- Penn State Health Milton S. Hershey Medical CenterRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
No Intervention
Active Comparator
Arm Label
No TENS unit use
TENS unit use
Arm Description
All subjects will start with 3 months of no TENS use and diary tracking
All subjects will then have 3 months of TENS use during episodes of endometriosis pain flare and diary tracking.
Outcomes
Primary Outcome Measures
Change in Average Daily VAS Pain Score
Average daily pain during endometriosis flares will be measured using a Visual Analog Scale (VAS), a horizontal line measuring pain from 0 (no pain) to 100 (worst pain), and compared between the baseline period (no TENS use) and treatment period (TENS use).
Secondary Outcome Measures
Change in Quality of Life Score from baseline to end of study using the EHP30 questionnaire
Change in quality of life from baseline to end of study using the Endometriosis Health Profile (EHP30) questionnaire. Scores range from 0 (best health status) to 100 (worst health status).
Change in Female Sexual Function Index Total Score using the FSFI questionnaire
Change in Female Sexual Function Index (FSFI) validated survey scores from baseline to end of study among participants who are currently partnered. FSFI total score ranges from 2.0 (poor) to 36.0 (best).
Full Information
NCT ID
NCT05348005
First Posted
December 8, 2021
Last Updated
April 3, 2023
Sponsor
Milton S. Hershey Medical Center
1. Study Identification
Unique Protocol Identification Number
NCT05348005
Brief Title
Use of TENS Unit in the Management of Endometriosis Pain
Official Title
A Cross-Over Study of the Use of Transcutaneous Electrical Nerve Stimulation Unit in the Management of Endometriosis Pain
Study Type
Interventional
2. Study Status
Record Verification Date
April 2023
Overall Recruitment Status
Recruiting
Study Start Date
July 28, 2022 (Actual)
Primary Completion Date
December 1, 2023 (Anticipated)
Study Completion Date
May 31, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Milton S. Hershey Medical Center
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.
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is see if Transcutaneous Electrical Nerve Stimulator (TENS) units help decrease endometriosis flare pain. TENS units have a 510K and are intended for relief of pain associated with sore or aching muscles of the lower back, arms, or legs due to strain from exercise or normal household and work activities.
Participants will complete surveys, record pain, medication use and bleeding in an online diary during endometriosis flare ups for 3 months without using the TENS unit. After the first 3 month period of time, a TENS unit will be given to participants to wear and again, record pain, medication use and bleeding in the online diary during endometriosis flare ups for and additional 3 months while using the TENS unit.
Detailed Description
The investigators propose to conduct a cross-over clinical study to evaluate the effectiveness of TENS units on the management of endometriosis flare-related pain. Subjects will participate in a 3-month "baseline" period (no TENS unit use for endometriosis flares) and then cross-over to a 3-month "treatment" period (TENS unit use for endometriosis flares).
Potential subjects will be pre-screened in the Penn State Minimally Invasive GYN (MIGS) Surgery Clinic for pathologically diagnosed endometriosis and from the Penn State MIGS endometriosis database. Potential subjects will then be called to evaluate the remainder of the inclusion and exclusion criteria. If fulfilled, potential subjects will follow up at the enrollment visit (Visit 1) where consent is reviewed and signed. The baseline QOL and FSFI REDCap surveys will be completed at this visit. Subjects will be set up to receive automated links to complete diary entries and surveys directly in REDCap.
Prior to initiating TENS unit use for endometriosis flare-related pain, subjects will record daily entries into RedCap during episodes of endometriosis flares for 3 months. Each entry will record their VAS pain score as well as medication intake and bleeding profile.
Subjects will then be mailed the TENS unit at the 3 months mark into the study. Subjects will then complete entries with TENS use at their discretion for the following 3 months and record TENS unit use duration, frequency, and side effects in addition to the documentation of pain, medication and bleeding. At the end of the study, subjects will complete a QOL and FSFI survey.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Endometriosis, Pelvic Pain
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Model Description
cross-over clinical study to evaluate the effectiveness of TENS units on the management of endometriosis flare-related pain. Subjects will participate in a 3-month "baseline" period (no TENS unit use for endometriosis flares) and then cross-over to a 3-month "treatment" period (TENS unit use for endometriosis flares).
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
40 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
No TENS unit use
Arm Type
No Intervention
Arm Description
All subjects will start with 3 months of no TENS use and diary tracking
Arm Title
TENS unit use
Arm Type
Active Comparator
Arm Description
All subjects will then have 3 months of TENS use during episodes of endometriosis pain flare and diary tracking.
Intervention Type
Device
Intervention Name(s)
Ovira Transcutaneous Electrical Nerve Stimulation Unit
Intervention Description
TENS units have a wide application from treatment of chronic back pain, chronic abdominal pain, cancer pain, perioperative pain, and labor pain.19-24 TENS units have been shown to be well-tolerated with minimal side effects and have been successful in reducing pain as well as pain medication use in patients with primary dysmenorrhea, which excludes pathology such as endometriosis. 11-18 Certain TENS units have also been FDA approved for the general indication of pelvic pain.
Primary Outcome Measure Information:
Title
Change in Average Daily VAS Pain Score
Description
Average daily pain during endometriosis flares will be measured using a Visual Analog Scale (VAS), a horizontal line measuring pain from 0 (no pain) to 100 (worst pain), and compared between the baseline period (no TENS use) and treatment period (TENS use).
Time Frame
Baseline Period (months 1-3) and Treatment Period (months 4-6)
Secondary Outcome Measure Information:
Title
Change in Quality of Life Score from baseline to end of study using the EHP30 questionnaire
Description
Change in quality of life from baseline to end of study using the Endometriosis Health Profile (EHP30) questionnaire. Scores range from 0 (best health status) to 100 (worst health status).
Time Frame
Baseline and 6 months
Title
Change in Female Sexual Function Index Total Score using the FSFI questionnaire
Description
Change in Female Sexual Function Index (FSFI) validated survey scores from baseline to end of study among participants who are currently partnered. FSFI total score ranges from 2.0 (poor) to 36.0 (best).
Time Frame
Baseline and 6 months
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Females ages 18-45 years at time of enrollment
A surgical diagnosis with direct visualization and/or histopathologic confirmation of endometriosis
Average monthly endometriosis pain flare
Naïve TENS user
Exclusion Criteria:
TENS device exclusion:
Implantable devices (pacemaker, Interstim, etc.)
Cardiac arrhythmia
Open skin sores over areas of placement
Pregnancy
Nursing or trying to conceive at this time
Post-operative <12 weeks from abdominal or pelvic surgery
Planned surgery or hormonal medication changes for duration of study if applicable
Non-English speaking or inability to read and understand English
Prisoners
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Linda Li, MD
Phone
7175310003
Ext
286762
Email
lindali@pennstatehealth.psu.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kristin W Riley, MD
Organizational Affiliation
Penn State Health Hershey Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Penn State Health Milton S. Hershey Medical Center
City
Hershey
State/Province
Pennsylvania
ZIP/Postal Code
17033
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Linda Li, MD
Phone
717-531-0003
Ext
286762
Email
lindali@pennstatehealth.psu.edu
First Name & Middle Initial & Last Name & Degree
Amyee McMonagle
Phone
7175314484
First Name & Middle Initial & Last Name & Degree
Linda Li, MD
First Name & Middle Initial & Last Name & Degree
Kristin Riley, MD
12. IPD Sharing Statement
Plan to Share IPD
No
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Use of TENS Unit in the Management of Endometriosis Pain
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