Attributes and Barriers to Care of Pelvic Pain in University Women

Mann J, Julie Mann, Shuster J, Jonathan J. Shuster, Jonathan Shuster, Nash Moawad, Nash S. Moawad
Journal of Minimally Invasive Gynecology · 2013 · vol. 20(6) , pp. 811–818 · doi:10.1016/j.jmig.2013.05.003 · PMID:23981982 · PMC4241758 · W2160398095
article OA: closed CC0 ⤵ 7 in-corpus citations
📄 Open PDF Full text JSON View on OpenAlex View on PubMed View at publisher
⚙ AI-generated summary by gemini-2.5-flash-lite+body, 2026-07-06 ⓘ

This study surveyed 390 female university students to assess the attributes and barriers to care for their pelvic pain experiences.

One-sentence paraphrase of the abstract; not a substitute for reading it. No clinical advice. How this works

⚙ AI-generated deep summary by claude@2026-07, 2026-07-06 · read from full text ⓘ

This cross-sectional survey assessed prevalence, symptom attributes, quality-of-life impact, and perceived barriers to care for chronic pelvic pain among a random sample of 2000 university women (18+), using an online questionnaire built in REDCap with established pelvic pain history and HRQOL-14 measures; 390 completed it (19.5% response rate). Among respondents, 72.8% reported some form of pelvic pain in the prior 12 months and these women had significantly worse physical and mental health, more limitation of activities, more sad days, and poorer sleep, while type-specific pain included premenstrual pain (65.1%) and deep dyspareunia among sexually active women (44.5%); a limitation was possible selection bias from low response and difficulty disentangling overlapping diagnoses. The study also found limited care access: only 26.4% of those with pelvic pain had seen a doctor, nearly 80% lacked diagnoses, few received medications or procedures, and reported barriers included insurance issues, perceived lack of physician knowledge, limited appointment access, and poor empathy. Relevance to endometriosis: the paper mentions endometriosis among the rare surgical procedures/conditions reported (excision of cysts and endometriosis), though the main focus is broad attributes and barriers to care of pelvic pain in university women rather than specifically endometriosis or adenomyosis.

Read from the paper's body, not the abstract. Not a substitute for reading the paper. No clinical advice. How this works

Abstract

Study objectiveTo describe rates of pelvic pain in university women ages 18 and older and to explore the barriers to adequate health care for pelvic pain in this population.DesignA cross-sectional study (Canadian Task Force classification II-2).SettingUniversity of Florida, Gainesville, FL.PatientsA total of 2000 female students at the University of Florida were randomly selected for participation.InterventionsThe 2000 sample members were sent a questionnaire to be completed online.Measurements and main resultsThe online questionnaire was hosted through the REDCap electronic data capture tool hosted at the University of Florida. This questionnaire included demographic items, general health and health behavior questions, measures to assess different types of pelvic pain (e.g., dysmenorrheal; dyspareunia; urinary, bowel, and vulvar pain), items regarding barriers to care for pelvic pain problems, and quality of life measures. Data were exported to SAS software (SAS Institute Inc., Cary, NC) for analysis. Of the 2000 subjects who received the questionnaire invitation, 390 filled out the questionnaire, yielding a response rate of 19.5%. Respondents' ages ranged from 18 to 62 with a mean of 23 years. A total of 72.8% of respondents reported experiencing pelvic pain over the past 12 months. Dysmenorrhea was reported by nearly 80% of participants, over one third of participants noted deep dyspareunia, and a significant proportion of participants reported symptoms related to bowel movements. Vulvar symptoms, including superficial dyspareunia, were reported by 21.5% of participants. Most participants with pelvic pain (78.8%) have not received any diagnosis for their pain, whereas 73.6% reported not yet having visited a doctor. Significant barriers to receiving adequate medical care were reported, including difficulty with insurance coverage and physicians' lack of time and knowledge or interest in chronic pelvic pain conditions.ConclusionPelvic pain in younger women is a critical public health issue experienced by a significant portion of the population. Significant awareness deficits and barriers to care exist. Careful study of the barriers to receiving adequate medical care reported by these women will allow researchers to describe how best to improve care for these syndromes.
Full text 16,531 characters · extracted from pmc-nxml · 3 sections · click to expand

Results

Of the 2000 random female students who received the survey via e-mail, 390 completed the survey for a 19.5% response rate. The mean age of this sample was 23 years (range, 18–62 years; standard deviation [SD] = 6.45). The majority of the sample (78.6%) identified themselves as white, with 9.6% identifying themselves as black or African American. The mean age of respondents’ first menstrual periods was 12.5 years (range, 9–16 years; SD = 1.37); 70.4% have used hormonal contraceptives beginning at a mean age of 17.9 years (range, 12–18 years, SD = 2.53) and using them for an average of 4.7 years (range, 0–30 years, SD = 4.34). Most respondents (90.1%) have never been pregnant, whereas 4.8% have been pregnant once and 5.1% have been pregnant 2 or more times; 9.6% of respondents reported ever having been diagnosed with a sexually transmitted infection. On average, per day, respondents reported consuming 1.25 cups of caffeine (range, 0–15; SD = 1.43), drinking .45 alcoholic drinks (range, 0–5; SD = .82), and smoking .11 cigarettes (range, 0–10; SD = .87). A total of 284 respondents (72.8% of total responses) reported they have experienced some form of pelvic pain in the previous 12 months. Those reporting pelvic pain were significantly younger (p = .020), with a mean age of 23 years compared with 25 years in those without pelvic pain. Three respondents were of postmenopausal age, but this did not significantly impact the statistical analysis. Of the 284 women reporting pelvic pain, premenstrual pain was the most common complaint (reported by 185 [65.1%]); pain after menstruation was reported by 38 (13.4%), deep dyspareunia by 97 (34.2%), deep pelvic pain after intercourse by 30 (10.6%), bowel-related pain by 109 (38.4%), and vulvar pain by 61 women (21.5%). When considering only sexually active women (218), deep dyspareunia was reported by 44.5% and deep pelvic pain after intercourse by 13.8%. Subjects reporting pelvic pain scored significantly worse on the CDC HRQOL-14 Healthy Days Measure in physical health (p = .013), mental health (p = .0014), limitation of activities (p<.001), the number of sad days per month (p = .013), poor sleep (p = .0019), and general health (p = .0027) ( Table 1 ). When searching for possible contributors to pelvic pain, there were no statistically significant differences between the group who reported pelvic pain and the group who reported no pelvic pain in terms of cigarette or caffeine use, age of first period, or the prevalence of other illnesses. Interestingly, women with pelvic pain reported fewer years of hormonal contraceptive use (p = .035) ( Table 2 ). There seemed to be an issue with seeking or accessing medical care in this population. Relatively few women with pelvic pain reported receiving adequate care. Only 75 of 284 of women who experienced pelvic pain (26.4%) reported having seen a doctor, and nearly 80% of respondents lacked diagnoses for their pain. Of the women with identified conditions, 45 of 59 (76.3%) were diagnosed in less than 6 months, and around 5% of women received incorrect diagnoses before they finally received accurate diagnoses. Most women reported never being prescribed any medication for their pelvic pain, whereas a small fraction (2.9%) has tried at least 3 different medications. Surgery was also uncommonly performed or offered, with only 7 respondents reporting diagnostic and/or therapeutic procedures, including colonoscopies, endoscopies, and excision of cysts and endometriosis. When asked what the greatest barrier was to receiving optimal care for their pelvic pain issues, 16.4% of respondents noted difficulty with insurance coverage; 11.8% cited perceived lack of physicians’ knowledge, training, or comfort managing their conditions; 9.6% noted perceived lack of physicians’ empathy or interest in their conditions; and 10.7% stated that they had difficulties getting appointments with appropriate physicians. Although barriers to care are difficult to further assess quantitatively, respondents provided descriptions of the difficulties they faced in searching for diagnoses and solutions for their pelvic pain. The authors present a representative sample of these responses here, many of which were provided by respondents who had not seen doctors. One respondent said she was scared to discuss her pelvic pain problem with a medical professional, whereas another stated she was embarrassed to go to a doctor because she usually waited for her urinary symptoms to improve instead of addressing the problem. Another respondent said she had not yet visited a doctor because she had spent time “thinking pain was normal.” One respondent, who reported having visited a doctor, felt her age was an issue, stating she “was young when it first started and it was difficult to talk about.” Another respondent cited a lack of personal knowledge regarding pelvic pain and insufficient funds to seek help as her greatest barriers. One woman who reported having seen at least 3 doctors for her pain felt her greatest barrier was a lack of agreement between her and her physician. Although she felt stress contributed to her irritable bowel syndrome symptoms, her gastroenterologist did not, and she was uncomfortable with her doctor’s suggestion to switch medications every few weeks to find something that worked. We found a striking difference in this random sample between the group who reported being sexually active and those who reported not being sexually active regardless of pelvic pain symptoms. Subjects who are sexually active reported lower scores on physical health, mental health, and the number of worried days ( Table 3 ). Among the students who reported pelvic pain, those who were sexually active (overall 76%) perceived their physical health and mental health to be worse (p<.001 and p = .040, respectively) than women who were not sexually active ( Table 4 ). Among the sexually active population in this study, women who reported pelvic pain perceived worse physical health (p = .0037) and mental health (p = .0095) and felt that these issues limited their usual activities more (p = .0013). They also reported more sad days per month (p = .023) and less rest or sleep (p<.001). However, this group did not perceive that their pain affected their day-to-day activities any more than did subjects not reporting pelvic pain (p = .42) ( Table 5 ). Among subjects without pelvic pain in the last 12 months, there was no difference in their perception of their physical health linked to whether they were sexually active or not. However, women without pelvic pain who were sexually active perceived their mental health to be worse (p = .036) ( Table 6 ). Overall, pelvic pain was associated with more problems in sexually active subjects than in those who are not sexually active ( Tables 5 and 7 ). Interestingly, even in women without pelvic pain, those who were sexually active reported lower perceived mental health scores ( Table 6 ).

Discussion

The results of this study suggest that pelvic pain, including pain with menstruation, intercourse, and bowel movements, is a significant problem for younger women. Pelvic pain does not appear to be associated with any of the demographic factors explored in this study; however, women experiencing pelvic pain perceived worse physical and mental health than women without pelvic pain. Moreover, being sexually active was linked with lower mental health scores regardless of pain status. It is impossible to ensure accurate identification of the prevalence of pelvic pain in this population. It is likely that this sample overrepresents women with pelvic pain because our response rate of 19.5% might have included more women who self-selected and felt the subject matter appealed to them because of their pain. It is not clear what the prevalence of pelvic pain is in subjects who chose not to respond to the survey. Additionally, many women may see this as a sensitive subject about which they prefer not to share information with researchers. Furthermore, the nature of symptoms can be confusing for women with or without diagnoses because many pelvic pain problems can have asymptomatic periods, can vary in severity, and can present overlapping symptoms; several pelvic pain conditions can also coexist [ 24 – 27 ]. Our study shows a lack of access to optimal health care for pelvic pain. Potential barriers to care included incompatibility with health care providers, finance and insurance issues, and a lack of understanding of these diseases or a lack of confidence in the need to seek help. It is also likely that the lack of patients’ awareness of pelvic health and the availability of effective and specialized care for such problems may be contributing to patients’ hesitation to seek care, particularly in their early reproductive years. This informational gap highlights the need for education and awareness to reach this population with accurate information regarding pelvic pain. Future research should explore associations between subtypes of pelvic pain and barriers to care because women with different symptoms may encounter different obstacles. In particular, university women may have a difficult time receiving adequate care because they are away from their primary care providers and families, and many of them are still covered under their parents’ health insurance, which may not provide adequate coverage if care is provided by out-of-network physicians. These issues may contribute to the greater diagnostic delays for adolescents (5.4 years as compared with 1.9 years for older adult women) observed by Greene et al [ 23 ], which may lead to the chronicity of pelvic pain and may render treatment more difficult [ 28 ]. It should be noted that although the respondents in this study attend university, higher education does not appear to protect women with pelvic pain from receiving delayed or inadequate care. Women with less education may fare even worse. Finally, quality of life poses a major problem for women with pelvic pain because this cohort reported lower scores for perceived physical and mental health status. This is consistent with the findings of Mathias et al [ 30 ] that women with pelvic pain had lower general health scores and more mood disturbances. Interestingly, Mathias et al also found that women with endometriosis reported the most distress relating to pain and its interference with daily activities. In future research, separating women by symptom type might yield similarly meaningful results. The interaction among pelvic pain conditions, sexuality, and perceived mental and physical health status in this study of university women is also enlightening. It will be valuable to examine the effect of treatment of pelvic pain on sexuality and quality of life measures in future research. This study benefited from the use of REDCap software allowing for a highly organized and precise measurement tool. Additionally, the automated data collection and export process ensured accuracy and minimized transcription errors. The content of the questionnaire was compiled from extensive research and widely used, validated measurement tools, such as the CDC’s HRQOL-14 Healthy Days Measure [ 32 ] and questionnaires on vulvodynia [ 33 ]. When validated surveys could not be found, items were drawn from the International Pelvic Pain Society’s Pelvic Pain Assessment form, which was compiled in 2008 based on a collaborative process with the International Pelvic Pain Society’s Board of Directors and clinician members. The questionnaire captured both quantitative and qualitative information from respondents. Unlike studies focused on patients presenting with pelvic pain, this sample was collected randomly from a cohort of average healthy women through the University of Florida’s Office of Institutional Planning and Research, which allowed for the comparison of women with and without pelvic pain. This study was limited by the inherent reporting bias associated with this cross-sectional study design. The response rate of 19.5% was low and might reflect a bias toward responses from women with pelvic pain issues. There were also few pain-free controls for the comparison of lifestyle factors and quality of life ratings. Future research can aim to reach larger, more comprehensive samples of women to ensure less reporting bias. Additionally, symptoms and diagnoses were self-reported and retrospective in nature, which limits the accuracy of the data collected. On the other hand, this study design is credited by the large, homogenous sample of educated young women and the anonymous electronic survey that avoided personal data collection on such a sensitive topic. We believe that this has allowed the survey to capture more candid responses and enlightening qualitative data that would have been challenging otherwise. In conclusion, the issue of pelvic pain is a pressing one for young women. Efforts can be made toward reaching optimal care for these women with a focus on providing useful information and increasing awareness about pelvic pain symptoms, disorders, and the available diagnostic and treatment options. Along with expanded research initiatives, this will hopefully contribute to greater quality of life for women suffering from chronic pelvic pain.

Materials|Methods

We conducted a cross-sectional study designed to assess CPP in female students attending the University of Florida, Gainesville, FL. A random sample of 2000 female students aged 18 years and older was selected and e-mailed a fairly extensive questionnaire about various attributes of pelvic pain as well as perceived barriers to care. The random sample was compiled by the University’s Office of Institutional Planning and Research. The Institutional Review Board of the University of Florida approved this study. The questionnaire was created using the REDCap electronic data capture tool hosted at the University of Florida [ 31 ]. REDCap (available at http://project-redcap.org/ ) is a secure application used to build and manage complex online surveys. With REDCap, the questionnaire was built with specifically designed fields to capture desired types of responses, a function used to transmit the hyperlink for this questionnaire to participants via e-mail, and automated export procedures for the collected data. Participants consented to participation electronically once they followed the hyperlink to the online questionnaire. The questionnaire included demographic items, general health and health behavior questions, measures to assess different types of pelvic pain (e.g., dysmenorrhea, dyspareunia, urinary, bowel, musculoskeletal, and vulvar), psychosocial factors, and items regarding barriers to care for pelvic pain problems. Some of these items were derived from the International Pelvic Pain Society’s History and Physical Form. Health-related quality of life (HRQOL) questions from the Center for Disease Control and Preventions’ HRQOL-14 Healthy Days Measure were included (2011). Branching logic was built into the survey to avoid redundancy and keep the subjects engaged, and to capture subject-specific information. For example, if participants note that they do not experience pelvic pain in the survey’s initial questions, they are directed via branching logic past the items detailing pelvic pain and directly to general health questions. Three reminder e-mails were sent to subjects over 8 weeks to optimize response rates. Data were exported from REDCap into SAS statistical package (SAS Institute Inc., Cary, NC). Quantitative and semiquantitative responses were compared by Satterthwaite corrected t tests. This allows us to compare the means between 2 groups even if the underlying variances are unequal. Because of the large sample sizes, where central limit theory applies, no distributional assumptions are made. General health is rated as excellent, very good, fair, or poor. Here the data are ordinal and analyzed by the Kruskal-Wallis test, also known as the Wilcoxon test, to compare the 2 groups. It needs to be noted that higher scores on the Healthy Days Measures represent worse outcomes despite the name of the instrument. Two-sided p values <.05 are considered significant. Although there is concern as to whether the survey responders are a generalizable sample, we did informally compare responders to the initial request for response (about 60% of the responding subjects) with those of the second request (about 40%). Their response distributions were quite similar.

Text is read by the "Ask this paper" AI Q&A widget below. Extraction quality varies by source — PMC NXML preserves structure cleanly, OA-HTML may include some navigation residue, and OA-PDF can have broken hyphenation. The publisher copy (via DOI) is the canonical version.

My notes (saved in your browser only)

⚙ Ask this paper AI returns verbatim quotes from the full text · source: pmc-nxml ⓘ

Answers must be backed by verbatim quotes from this paper's full text. Hallucinated quotes are dropped automatically; if no verbatim passage answers the question, we say so. How this works

Citation neighborhood

Papers in the corpus that this work cites (lower rings, blue) and that cite this one (upper rings, green). Dot size scales with the paper's in-corpus citation count — bigger dot = more influential within the endo/adeno field. Click a dot to open that paper. [ expand to 2 hops ] — adds papers reached through this work's immediate citers/citees. Heavier; up to 60 extra dots.

References (65)

Cited by (9)

Source provenance

crossref
last seen: 2026-06-13T06:42:45.190161+00:00
europepmc
last seen: 2026-08-30T09:23:35.175841+00:00
openalex
last seen: 2026-06-10T17:14:06.276822+00:00
unpaywall
last seen: 2026-09-04T06:34:25.427880+00:00
License: CC0 · commercial use OK