The goal of this research is to improve pain outcomes for the over 500K Canadian women, girls and gender-diverse individuals who are newly diagnosed with endometriosis each year. Chronic pain that persists after interventions for endometriosis is a huge problem. There is some evidence that endometriosis-associated pain (EAP) is, at least to some extent, associated with changes in pain physiology, particularly central sensitization of pain. There is currently no effective evidence-informed intervention that addresses EAP. Yet a recent feasibility trial on a repetitive transcranial magnetic stimulation (rTMS) intervention demonstrated promising results compared to a sham intervention for reducing pain in a sample with EAP. The objectives of this trial are: 1. to evaluate the effectiveness of an rTMS intervention for pain reduction among those with recalcitrant post-operative EAP, 2. to inform on the utility of a long (10 session) vs short (5 session) protocol for pain reduction among those with recalcitrant post-operative EAP 3. to determine if any improvements in pain observed 30 days after an rTMS intervention are retained 6 months later 4. to identify physical and psychosocial mediators that impact the successful reduction of pain among patients with EAP treated using rTMS. 5. to describe patients' perceptions of and satisfaction with rTMS as an intervention for EAP.
This will be a double-blind, randomized-controlled trial (RCT) using a 2X2 factorial design. The protocol was developed following the Consolidated Standards of Reporting Trials (CONSORT) statement and also follows the Canadian Institutes for Health Research (CIHR) Strategy for Patient-Oriented Research (SPOR) to adapt research activities and dissemination strategies to patients equitably and effectively. The interventions include repetitive transcranial magnetic stimulation (rTMS) delivered using either a real or a sham coil and one of two intervention durations (short: 5-session, long: 10 session), thus four study groups with 1:1:1:1 allocation. Intervention: The rTMS intervention will be delivered to the primary motor cortex (M1) on the left side, over the hand representation using high frequency (HF) rTMS. Since there is no known somatotopy for pelvic pain, handedness is not thought to be important, however, handedness will be recorded to verify this. The rTMS intervention will be applied by way of a Magstim Rapid² system (Whitland, UK) coupled with a 70mm cooled figure-of-8 coil. The coil position and orientation will be standardized between treatment visits through using a Brainsight neuronavigation system (Rogue Research, Canada). A standard Montreal Neurological Institute (MNI) atlas will be used. The stimulation target will be individually defined at baseline as the site eliciting the highest averaged motor evoked potential (MEP) peak-to-peak amplitude in the first dorsal interosseous (FDI) muscle. The resting motor threshold (RMT) will be defined as the lowest intensity stimulus that elicits a MEP in the FDI of the right hand, with a peak-to-peak amplitude of at least 50 uV in 50% of trials. MEPs will be recorded using the on-board EMG system. Each rTMS session (real or sham) will consist of a total of 1500 pulses: 15 sets of pulses delivered at 10Hz for 10s at 80% RMT, separated by 50s intervals. The short protocol will involve interventions on 5 consecutive days, while the long protocol will include a 2-day break and another 5- day intervention. Acceptability, adverse events and side effects will be recorded after each session. Missed visits will be rescheduled wherever possible (but tracked). and adherence will be recorded as a proportion of sessions attended. Participant allocation: Concealed, computer-generated allocation will be performed using permuted block randomization (block size= 4) only after a participant has consented and completed all questionnaires at baseline. The allocation sequence will be managed by an independent investigator not associated with the project. It will be concealed from the study team through storage in a password protected file on an encrypted computer, backed up in a password-protected directory. Groups will be labelled as A-short, A-long, B-short, B-long, to keep investigators and participants blinded as to which coil (A/B) provides real/sham rTMS (only one investigator who will have no direct involvement with participants will know which coil provides real/sham rTMS; they look, sound and feel identical). Treatment duration will be revealed only to the recruitment officer, to the individual delivering the intervention, and the participant, since they will need to know the length of the protocol to schedule intervention sessions and follow-up. Gender will be recorded and if possible, gender-based sub-analyses will be performed. the sample will not be stratified by race/ethnicity, however efforts will be made to ensure diversity in the sample, as the prevalence of endometriosis also appears to be influenced by race/ethnicity. Recruitment bias will be minimized through using multiple recruitment sources with broad reach. Consistent with the CONSORT extension recommendations for trials involving non-pharmacological interventions, the researchers who perform baseline and follow-up assessments will not be involved in the treatment, and will be blinded to group allocation. Data collection: A series of questionnaires will be completed using an on-line platform before and after the intervention and laboratory-based assessments will occur on the day of the first and final (5th or 10th) intervention session, at the later of which participants will report their patient global impression of change (PGIC) in pain, and their patient satisfaction with treatment (PST). All participants will be followed daily to record their daily pain (NRS 0-10) in the 30 days before the first and 30 days after the last rTMS intervention session using automated text messaging or e-mail notifications, or phone calls if that is their preference. 30 days after the intervention (primary end point), and 6 months later, participants will provide their PGIC for pain, PST, and complete the Brief Pain inventory (BPI), the Endometriosis Health Profile (EHP-30) and the Beck Depression Index (BDI), through an on-line platform (reminders will be sent and non-completion will be monitored, with follow-up by the protocol officer to ensure completion wherever possible). Individuals randomized to the real intervention (both short and long protocols) will be invited to participate in a semi-structured interview through which we aim to capture a nuanced impression of the effectiveness of the intervention, its acceptability, and other observations. Target Sample size: The target sample size is 152 participants (38 per group). The sample size was estimated based on findings of a prospective cohort study by Pinot-Monange et al. which suggested that 75% of participants (9 of 12) will be improved on the PGIC, and that there will be a reduction in reported pain sensitivity (d=0.62) associated with the short rTMS protocol. The rTMS literature suggests that a moderate effect size (Cohen's d=0.05), will be achieved, suggesting that a sample of 30 per group will provide sufficient power to detect an intervention effect. A simulation in R based on 100 replications using a small (d=0.2) effect suggested that such an interaction would be detected (power = 0.80) with a sample size of n=100 (25 per group). The sample size includes estimated conservative drop-out rates, 15%, at the primary end point, and 25% after 6 months. Recruitment sources: Recruitment will be from a broad range of sources within the Ottawa, Ontario and Gatineau Quebec regions of Canada, including local gynecology clinics, local physiotherapy clinics, social media platforms (Instagram, X, Facebook), printed posters at sites within the community related to social interests, cultural practices, and religious beliefs, and sexual health resource centers. Planned analyses: Baseline participant characteristics will be aggregated by group and summarized using descriptive statistics. Intent-to-treat analyses will be performed to address Objectives 1-3. To answer Objectives 1 and 2, and to address relevant secondary objectives, 2-way repeated-measures ANOVAs will be performed for continuous variables, including intervention (2 levels: real, sham) and duration (2 levels: short, long) as main effects, and the interaction between intervention and duration, using α=0.05 and adjusting for unequal variances if necessary. Where there are significant interaction effects, Cohen's d and marginal means will be used to estimate effect sizes. Where no significant interactions are found, within- and between-group main effects will be estimated using Cohen's d. Chi-Square analyses will be used to evaluate group differences in the proportion of participants reporting meaningful clinical changes in pain based on the average daily pain (\>30% improvement) and the PGIC (somewhat to very much improved), generating Odds Ratios and estimating the number needed to treat with 95% confidence. Analyses after the 6- month follow-up will include time as a main effect. Wherever possible, the data will be disaggregated by gender and race/ethnicity, and sub-analyses will be performed. Where this is not possible, descriptive analyses by gender and race/ethnicity will be reported, highlighting observations that may inform future studies. To address Objective 4, univariate analyses using only data from those who received real rTMS will be used to identify trends (p\<0.15) in baseline and demographic data such as, age, race, gender, daily pain, EHP-30, BPI, Central Sensitization Inventory (CSI), Pain Catastrophizing Scale (PCS), BDI, State Trait Anxiety Inventory (STAI), pressure pain threshold (PPThresh), pressure pain tolerance (PPTol), temporal summation of pain (TS), conditioned pain modulation (CPM) and Tampon Test, suggestive of differences between successes (\>30% improvement) and failures. Separate binary logistic regression models will examine the relationship between independent variables tending to differ by group and clinically relevant improvements in dependent variables \[PGIC (somewhat to very much improved), daily pain (\>30% improved), BPI (\> 30% improved) and EHP-30(\> 30% improved). Only three predictors will be included in the final model- the one's with the largest effect sizes in univariate testing. Bootstrapping (X1000) will be used to improve the robustness of the models. Recruitment rate, adherence, adverse events and use of rescue medications (reported on the BPI) will be analyzed descriptively, and any protocol deviations will be described. Post-intervention interview data will be coded, and a thematic analysis will be completed in duplicate using N-Vivo software. Interviews will continue until 15 have been completed, thematic saturation is reached, and no new themes emerge after three consecutive interviews. Planned Interim analyses: One interim analysis will be performed once n=16 per group have reached the primary endpoint and based on Question 1. The trial will be deemed futile if the conditional power to detect a treatment effect for all intervention groups is \<30%. The trial will not be deemed futile based on the power of the interaction effect.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
152
5 consecutive treatment sessions will be provided using a protocol based on the updated guideline (Lefaucheur, 2014) and on Pinot-Monange et al. (2019). Each treatment session will last approximately 30 minutes. Acceptability, adverse events and side effects will be recorded after each session, while the researchers will also record the total treatment time, difficulties encountered during implementation, and any modifications to the intervention.
5 consecutive sham treatment sessions will be provided using a protocol based on the updated guideline (Lefaucheur, 2014) and on Pinot-Monange et al. (2019). Each treatment session will last approximately 30 minutes. Acceptability, adverse events and side effects will be recorded after each session, while the researchers will also record the total treatment time, difficulties encountered during implementation, and any modifications to the intervention
10 consective treatment sessions will be provided using a protocol based on the updated guideline (Lefaucheur, 2014) and on Pinot-Monange et al. (2019). Each treatment session will last approximatly 30 minutes. Acceptability, adverse events and side effects will be recorded after each session, while the researchers will also record the total treatment time, difficulties encountered during implementation, and any modifications to the intervention.
10 consective sham treatment sessions will be provided using a protocol based on the updated guideline (Lefaucheur, 2014) and on Pinot-Monange et al. (2019). Each treatment session will last approximatly 30 minutes. Acceptability, adverse events and side effects will be recorded after each session, while the researchers will also record the total treatment time, difficulties encountered during implementation, and any modifications to the intervention.
McLean Function Measurement Lab
Ottawa, Ontario, Canada
RECRUITINGNumeric rating scale (NRS) used to record daily pain over 30 days
Pain intensity, using a numeric rating scale (NRS), will be recorded daily for 30 days prior to trial entry to provide a suitable baseline, It will measure the average and worst overall pain intensity, menstrual and sexual activity related pain (if applicable). The questions will be applied as described below: Please rate any pain you experienced today (over the past 24 hours) that you attribute to your endometriosis using a scale from 0 (no pain) to 10 (worst pain imaginable). Is today your first day of menstrual cycle? Did you attempt any sexual activity or tampon insertion in the last 24hs? Please rate the pain associated with this activity on a scale from 0 (no pain) to 10 (worst pain imaginable),for sexual activity and/or tampon insertion (if applicable).
Time frame: Baseline -30 days after enrolment and before allocation
Numeric rating scale(NRS) used to record daily pain over 30 days
Pain intensity, using a numeric rating scale (NRS), will be recorded daily after the intervention period for 30 days. It will measure the average and worst overall pain intensity, menstrual and sexual activity related pain (if applicable). The questions will be applied as described below: Please rate any pain you experienced today (over the past 24 hours) that you attribute to your endometriosis using a scale from 0 (no pain) to 10 (worst pain imaginable). Is today your first day of menstrual cycle? Did you attempt any sexual activity or tampon insertion in the last 24hs? Please rate the pain associated with this activity on a scale from 0 (no pain) to 10 (worst pain imaginable), for sexual activity and/or tampon insertion (if applicable).
Time frame: 30 days following intervention
Patient Global Impression of Change (PGIC) in pain
PGIC is a single question through which participants provide a ordinal rating based on their overall perception of change in their pain attributed to the intervention: Very Much Better, Much Better, Somewhat better, About the same, somewhat worse, much worse, very much worse
Time frame: After the Intervention on the final intervention day
Patient Global Impression of Change (PGIC) in pain
PGIC is a single question through which participants provide a ordinal rating based on their overall perception of change in their pain attributed to the intervention: Very Much Better, Much Better, Somewhat better, About the same, somewhat worse, much worse, very much worse
Time frame: 30 days after completing the intervention
Patient Global Impression of Change (PGIC) in pain
PGIC is a single question through which participants provide a ordinal rating based on their overall perception of change in their pain attributed to the intervention: Very Much Better, Much Better, Somewhat better, About the same, somewhat worse, much worse, very much worse
Time frame: 6 months after the intervention
The Beck Depression Inventory (BDI-II)
The 21-item self-administered survey is scored on a scale of 0-3 in a list of four statements arranged in increasing severity about a symptom of depression. BDI-II assesses presence and intensity of mood symptoms. The scale can be divided into 2 subscales, affective symptoms (8 items) and somatic symptoms (13 items). Cut-off scores are available to classify degree of mood intensity. There is a four-point scale for each item ranging from 0 to 3. On two items (16 and 18) there are seven options to indicate either an increase or decrease of appetite and sleep. Cut-off score guidelines for the BDI-II are given with the recommendation that thresholds be adjusted based on the characteristics of the sample, and the purpose for use of the BDI-II. Total score of 0-13 is considered minimal range, 14-19 is mild, 20-28 is moderate, and 29-63 is severe. This scale can be scored either manually or using the Pearson proprietary software Q-global.
Time frame: Baseline
The Beck Depression Inventory (BDI-II)
The 21-item self-administered survey is scored on a scale of 0-3 in a list of four statements arranged in increasing severity about a symptom of depression. BDI-II assesses presence and intensity of mood symptoms. The scale can be divided into 2 subscales, affective symptoms (8 items) and somatic symptoms (13 items). Cut-off scores are available to classify degree of mood intensity. There is a four-point scale for each item ranging from 0 to 3. On two items (16 and 18) there are seven options to indicate either an increase or decrease of appetite and sleep. Cut-off score guidelines for the BDI-II are given with the recommendation that thresholds be adjusted based on the characteristics of the sample, and the purpose for use of the BDI-II. Total score of 0-13 is considered minimal range, 14-19 is mild, 20-28 is moderate, and 29-63 is severe. This scale can be scored either manually or using the Pearson proprietary software Q-global.
Time frame: 30 days following the intervention
The Beck Depression Inventory (BDI-II)
The 21-item self-administered survey is scored on a scale of 0-3 in a list of four statements arranged in increasing severity about a symptom of depression. BDI-II assesses presence and intensity of mood symptoms. The scale can be divided into 2 subscales, affective symptoms (8 items) and somatic symptoms (13 items). Cut-off scores are available to classify degree of mood intensity. There is a four-point scale for each item ranging from 0 to 3. On two items (16 and 18) there are seven options to indicate either an increase or decrease of appetite and sleep. Cut-off score guidelines for the BDI-II are given with the recommendation that thresholds be adjusted based on the characteristics of the sample, and the purpose for use of the BDI-II. Total score of 0-13 is considered minimal range, 14-19 is mild, 20-28 is moderate, and 29-63 is severe. This scale can be scored either manually or using the Pearson proprietary software Q-global.
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Time frame: 6 months following the intervention
The State-Trait Anxiety Inventory (STAI)
The State-Trait Anxiety Inventory (STAI) (Stauder, 2003) allows discrimination between anxiety as a personality trait (STAI-T) or as an emotional response to a situation (STAI-S). This 40-item scale has shown a good reliability, consistency, and responsiveness (Sepulcri, 2009). Using the STAI, Sepulcri \& do Amaral (Sepulcri, 2009) reported that 87.5% of patients with EAP reported anxiety, with significant associations between both STAI-T and STAI-S and pain intensity. Total scores for state and trait are calculated, ranging from 20 - 80. Higher scores indicate greater anxiety. 1. = Scores between 20-39 means "no or low anxiety" 2. = Scores between 40-59 means "moderate anxiety" 3. = Scores between 60-80 means "high anxiety"
Time frame: Baseline
The Pain Catastrophizing Scale
This is a reliable and valid scale to measure of catastrophizing. The scores from this questionnaire is predictors of intensity of physical and emotional distress. It is a self-report measure, consisting of 13 items scored from 0 to 4, resulting in a total possible score of 52. The higher the score, the more catastrophizing thoughts are present.
Time frame: Baseline
The Central sensitization index
The Central Sensitisation Inventory (CSI) is a self-report outcome measure designed to identify patients who have symptoms that may be related to central sensitisation (CS) or central sensitivity syndromes (CSS). Part A includes 25 questions related to common CSS symptoms. Part B determines if the patient has been diagnosed with certain CSS disorders or related disorders, such as anxiety and depression. CSI severity levels have been established for part A: subclinical = 0 to 29; mild = 30 to 39; moderate = 40 to 49; severe = 50 to 59; and extreme = 60 to 100.
Time frame: Baseline
Female Sexual Distress Scale (FSDS)
The Female Sexual Distress Scale-Revised (FSDS-R) is a 13-item questionnaire designed to assess sexually related distress in women with hypoactive sexual desire disorder (HSDD). It has been validated for evaluating distress associated with inadequate or impaired sexual function. The total score on the FSDS-R ranges from 0 to 48, with higher scores indicating higher levels of sexual distress. A cutoff score of 15 or more is recommended for determining the presence of personal sexual distress.
Time frame: Baseline
Adherence to the intervention protocol
Attendance of rTMS treatment visits will be tracked (%).
Time frame: During intervention sessions
Pressure pain threshold (PPThresh)
PPT will be determined using an algometer device in three regions over the lower abdomen \[lower left and right quadrants (4cm medial to the anterior superior iliac spine) and midline (1 cm superior to the midline pubic symphysis)\]. Three sites remote to the pelvis (right thenar eminence, right upper trapezius, and right medial gastrocnemius) will also be assessed. PPT will be defined as the median pressure (Newton), among three trials, at which participants first report pain. After each pressure application participants will be asked to rate their pain using the NRS from 0 to 10.
Time frame: Baseline before allocation
Pressure pain threshold (PPThresh)
PPT will be determined using an algometer device in three regions over the lower abdomen \[lower left and right quadrants (4cm medial to the anterior superior iliac spine) and midline (1 cm superior to the midline pubic symphysis)\]. Three sites remote to the pelvis (right thenar eminence, right upper trapezius, and right medial gastrocnemius) will also be assessed. PPT will be defined as the median pressure (Newton), among three trials, at which participants first report pain. After each pressure application participants will be asked to rate their pain using the NRS from 0 to 10.
Time frame: After the final intervention session on the same day as that session
Pressure Pain Tolerance (PPTol)
PPTol will be determined using an algometer device in three regions over the lower abdomen \[lower left and right quadrants (4cm medial to the anterior superior iliac spine) and midline (1 cm superior to the midline pubic symphysis)\]. Three sites remote to the pelvis (right thenar eminence, right upper trapezius, and right medial gastrocnemius) will also be assessed. PPTol will be defined as the median pressure (Newton), among three trials, at which participants can tolerate the pressure before the sensation becomes intolerable or unbearable. After each pressure application participants will be asked to rate their pain in a numerical rating scale (NRS) from 0 to 10.
Time frame: Baseline before allocation
Pressure Pain Tolerance (PPTol)
PPTol will be determined using an algometer device in three regions over the lower abdomen \[lower left and right quadrants (4cm medial to the anterior superior iliac spine) and midline (1 cm superior to the midline pubic symphysis)\]. Three sites remote to the pelvis (right thenar eminence, right upper trapezius, and right medial gastrocnemius) will also be assessed. PPTol will be defined as the median pressure (Newton), among three trials, at which participants can tolerate the pressure before the sensation becomes intolerable or unbearable. After each pressure application participants will be asked to rate their pain in a numerical rating scale (NRS) from 0 to 10.
Time frame: Immediately after the final intervention session
Perceived pain intensity (PPI)
Perceived pain intensity (PPI) will be applied, using an algometer device during 5 seconds using the mean pressure between PPThresh and PPTol obtained previously for each participant, in all sites described above. After each pressure application participants will be asked to rate their pain in a numerical rating scale (NRS) from 0 to 10.
Time frame: Baseline before allocation
Perceived pain intensity (PPI)
Perceived pain intensity (PPI) will be applied, using an algometer device during 5 seconds using the mean pressure between PPThresh and PPTol obtained previously for each participant, in all sites described above. After each pressure application participants will be asked to rate their pain in a numerical rating scale (NRS) from 0 to 10.
Time frame: Immediately after the final intervention session
Temporal summation (TS) of pain
TS is reflective of sensitization through peripheral and/or central mechanisms. The stimulus intensity will be the PPI determined above at the midline lower abdominal site and at the thenar site, determined during pressure pain threshold (PPT) assessment. Ten stimuli will be delivered at each site at a rate of one per second. Pain intensity reported using a NRS, induced by the application of the stimulus on the 1st and 10th application will be recorded. TS will be considered as a dichotomous variable, deemed to be present if there is a positive difference \> 1 between NRS ratings on the tenth minus that of the first application of the stimulus and negative otherwise
Time frame: Baseline before allocation
Temporal summation (TS) of pain
TS is reflective of sensitization through peripheral and/or central mechanisms. The stimulus intensity will be the PPI at the lower abdominal site and at the thenar site, determined during pressure pain threshold (PPT) assessment. Ten stimuli will be delivered at each site at a rate of one per second. Pain intensity reported using a NRS, induced by the application of the stimulus on the 1st and 10th application will be recorded. TS will be considered as a dichotomous variable, deemed to be present if there is a positive difference \> 1 between NRS ratings on the tenth minus that of the first application of the stimulus and negative otherwise
Time frame: Immediately after the final intervention session
Pain rating during the tampon test
The participants will be provided with Original Regular Tampax Tampon and will be instructed to insert and then remove it. After, they will be asked to record the degree of pain during the entire insertion/removal experience in a 11-point numerical rating scale (NRS) with anchors of 0 (no pain at all) to 10 (worst pain imaginable).
Time frame: Baseline before allocation
Pain rating during the tampon test
The participants will be provided with Original Regular Tampax Tampon and will be instructed to insert and then remove it. After, they will be asked to record the degree of pain during the entire insertion/removal experience in a 11-point numerical rating scale (NRS) with anchors of 0 (no pain at all) to 10 (worst pain imaginable).
Time frame: Immediately after the final intervention session
Conditioned pain modulation (CPM)
CPM is manifested by a reduction in pain perception in one location through the simultaneous application of a painful stimulus at a distant, non-segmental location on the body. A lack of CPM is reflective of decreased descending endogenous pain inhibition, a contributor to central sensitization. Through the PPThresh (test stimulus) will be tested at the lower midline abdominal site and the thenar eminence site. A blood pressure cuff will be applied to the dominant upper arm and inflated at a rate of 20 mmHg/s until the participant reports a pain intensity of 3/10 (conditioning stimulus). The test stimulus will be repeated 3X at each site while the pressure is retained at the upper arm. CPM will be deemed present if the median PPThresh is lower with the conditioning stimulus applied than prior to the conditioning stimulus.
Time frame: Baseline before allocation
Conditioned pain modulation (CPM)
CPM is manifested by a reduction in pain perception in one location through the simultaneous application of a painful stimulus at a distant, non-segmental location on the body. A lack of CPM is reflective of decreased descending endogenous pain inhibition, a contributor to central sensitization. Through the PPThresh (test stimulus) will be tested at the lower midline abdominal site and the thenar eminence site. A blood pressure cuff will be applied to the dominant upper arm and inflated at a rate of 20 mmHg/s until the participant reports a pain intensity of 3/10 (conditioning stimulus). The test stimulus will be repeated 3X at each site while the pressure is retained at the upper arm. CPM will be deemed present if the median PPThresh is lower with the conditioning stimulus applied than prior to the conditioning stimulus.
Time frame: Immediately after the final intervention session
The Brief Pain Inventory
It evaluates a patient's pain experience over the previous 1 weeks through locating the pain, noting medication or other interventions, and 11 different numeric rating scales (NRSs) ask about pain intensity (current, least, most, and average for the past 24 hours) and the effect of the pain on function during various activities of daily living. The BPI is an excellent tool for monitoring the effect of pain or treatment of pain, or both, in terms of a patient's functional ability or disability over time. Cronbach alpha reliability ranges from 0.77 to 0.91. Scoring: The short version of the BPI (Short form) includes 9 items. It uses a 0 to 10 numeric rating scales for item rating. Pain Score: * 1 - 4 = Mild Pain * 5 - 6 = Moderate Pain * 7 - 10 = Severe Pain
Time frame: Baseline before allocation
The Brief Pain Inventory
It evaluates a patient's pain experience over the previous 7 days through locating the pain, noting medication or other interventions, and 11 different numeric rating scales (NRSs) ask about pain intensity (current, least, most, and average for the past 24 hours) and the effect of the pain on function during various activities of daily living. The BPI is an excellent tool for monitoring the effect of pain or treatment of pain, or both, in terms of a patient's functional ability or disability over time. Cronbach alpha reliability ranges from 0.77 to 0.91. Scoring: The short version of the BPI (Short form) includes 9 items. It uses a 0 to 10 numeric rating scales for item rating. Pain Score: * 1 - 4 = Mild Pain * 5 - 6 = Moderate Pain * 7 - 10 = Severe Pain
Time frame: 30 days after the final intervention session
The Brief Pain Inventory
It evaluates a patient's pain experience over the previous 1 weeks through locating the pain, noting medication or other interventions, and 11 different numeric rating scales (NRSs) ask about pain intensity (current, least, most, and average for the past 24 hours) and the effect of the pain on function during various activities of daily living. The BPI is an excellent tool for monitoring the effect of pain or treatment of pain, or both, in terms of a patient's functional ability or disability over time. Cronbach alpha reliability ranges from 0.77 to 0.91. Scoring: The short version of the BPI (Short form) includes 9 items. It uses a 0 to 10 numeric rating scales for item rating. Pain Score: * 1 - 4 = Mild Pain * 5 - 6 = Moderate Pain * 7 - 10 = Severe Pain
Time frame: 6 months after the final intervention session
The Endometriosis Health Profile Questionnaire (EPH-30)
The 30 questions of the EHP-30 involve five scales (pain, control and powerlessness, emotional well-being, social support, and self-image) answered based on a 4-week recall period. Higher scores (/100) reflect better health.
Time frame: Baseline before allocation
The Endometriosis Health Profile Questionnaire (EPH-30)
The 30 questions of the EHP-30 involve five scales (pain, control and powerlessness, emotional well-being, social support, and self-image) answered based on a 4-week recall period. Higher scores (/100) reflect better health.
Time frame: 30 days after the final intervention session
The Endometriosis Health Profile Questionnaire (EPH-30)
The 30 questions of the EHP-30 involve five scales (pain, control and powerlessness, emotional well-being, social support, and self-image) answered based on a 4-week recall period. Higher scores (/100) reflect better health.
Time frame: 6 months after the final intervention session
Patient satisfaction with treatment (PST)
Global patient satisfaction with treatment is a single question through which participants provide their rating of satisfaction using a scale from zero to ten. Higher ratings reflect greater satisfaction.
Time frame: Immediately after the intervention on the final day of the intervention
Patient satisfaction with treatment (PST)
Global patient satisfaction with treatment is a single question through which participants provide their rating of satisfaction using a scale from zero to ten. Higher ratings reflect greater satisfaction.
Time frame: 30 days after the final intervention session
Patient satisfaction with treatment (PST)
Global patient satisfaction with treatment is a single question through which participants provide their rating of satisfaction using a scale from zero to ten. Higher ratings reflect greater satisfaction.
Time frame: 6 months after the final intervention session