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Despite how common inguinal hernia repair (IHR) surgery is, there is little research on how best to prepare people for this operation. Surgeons' advice to patients about exercise and physical activity are inconsistent and usually based on their clinical opinion. Some surgeons recommend exercise to help prepare for the operation while others say to rest. Research is needed to help know whether exercise is helpful before and after IHR surgery.
This study will observe the effects of education and exercise before and immediately after IHR surgery. Half of the participants will be randomized to an education and exercise group and the other half to a non-exercise, care as usual group. Participant outcomes will be measured up to 3 months after their surgery. It is expected that participants in the education and exercise group will have: 1) less pain at follow-up, 2) better hernia-related outcomes, 3) quicker return to activity and work, and 4) improved overall experience surrounding IHR surgery. This project will help in developing clear guidelines for pre- and post-operation to better prepare patients for IHR surgery.
Inguinal hernia repair (IHR) surgery is one of the most common surgeries performed globally, with more than 20 million procedures annually. Despite the frequent occurrence of this condition and consequent surgical repair, patient outcomes for IHR need improvement; the rate of hernia recurrence following surgical repair is approximately 15% and an estimated 10-12% of patients undergoing this surgery have chronic post-surgical pain that lasts months or years. Poor surgical outcomes negatively affect individual patients who experience pain, activity limitation, and decreased quality of life. This also results in significant burden on employers and healthcare systems through decreased productivity, lost time at work, and an increased number of appointments.
Even though IHR is incredibly common, there is a lack of quality literature investigating the effects and safety of physical activity surrounding this condition. This results in recommendations given to patients that are variable, inconsistent, and largely based upon clinical opinion. Evidence from related surgical procedures suggests that preoperative exercise and education (prehabilitation), followed by postoperative rehabilitation may result in better outcomes following surgery. Though initially argued for orthopedic procedures and adopted to cardiovascular and pulmonary surgical procedures, the use of prehabilitation is spreading to other surgical subspecialties as well. One study observed that improved preoperative physical functioning as defined by a timed stair climbing task was associated with fewer postoperative complications in patients waiting to undergo major abdominal surgery and was a better predictor of perioperative complications than other risk factors such as chronic comorbidities, tobacco use, or alcohol abuse. A recent systematic review found that surgery type may not actually be an important modifier of prehabilitation efficacy, and that the benefits of prehabilitation span multiple surgical.
Perioperative rehabilitation for IHR is supported mainly by limited and indirect evidence. A study in 2018 was the first randomized controlled trial to examine the impact of a weight loss centered prehabilitation program on patients waiting to undergo ventral hernia repair and found improved hernia- and complication-free rates in the prehabilitation group following surgery, but also higher dropout and emergent repair rates in the prehabilitation group, raising safety concerns. A two-year follow-up study found no significant long-term differences in complications or sustained weight loss between standard care and prehabilitation groups. No studies currently combine prehabilitation and post-operative rehabilitation, or inform recovery time, post-surgical pain, and return to activity after inguinal hernia repair. Pain catastrophizing and fear of movement appear to be important predictors of postsurgical outcomes. Due to a lack of quality literature, recommendations given to patients that are based on clinical opinion that encourage limiting physical activity for extended periods of time can encourage unhelpful beliefs about pain, fear of movement and poor coping strategies. Research is needed to inform practice guidelines and return-to-activity recommendations.
This research team previously conducted a pilot study investigating the feasibility of a study investigating perioperative rehabilitation for IHR and discovered that a larger study is feasible in terms of recruitment, assessment, and protocol implementation. The investigators are now moving forward to a larger randomized controlled trial (RCT) with improvements and refinements to the protocol.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Intervention Group | Experimental | 49 participants will be randomly selected to the intervention group. These participants will receive six weeks of pre-operative exercise and education, as well as six weeks of graduated post-operative exercise instruction, beginning at three weeks post-op with the surgeon's clearance. |
|
| Control Group | No Intervention | 49 participants will be randomly selected to the control group. These participants will receive pre-operative education in the form of educational videos. They will not receive exercise instruction. |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Rehabilitation | Other | Pre- and post-operative exercise and education. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Self-reported pain due to hernia | Pain as measured on the Pain Disability Index, scored 0-10, with 0 being no pain and 10 being the worst pain. | From enrollment to 12 weeks post-op |
| Measure | Description | Time Frame |
|---|---|---|
| Hernia Recurrence | At 12 weeks post-op | |
| Return to regular work/activity | From enrollment to 12 weeks post-op | |
| Surgical experience |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Anna Shologan | Contact | 780-492-2690 | asholo@ualberta.ca | |
| Douglas Gross | Contact | 780-492-2690 | dgross@ualberta.ca |
| Name | Affiliation | Role |
|---|---|---|
| Douglas Gross | University of Alberta | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of Alberta | Edmonton | Alberta | Canada |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| Background | Canadian Society for Exercise Physiology (CSEP). 2017. Get Active Questionnaire[Online] Available from https://csep.ca/2021/01/20/pre-screening-for-physical-activity/. | ||
| 12514456 | Background | Poobalan AS, Bruce J, Smith WC, King PM, Krukowski ZH, Chambers WA. A review of chronic pain after inguinal herniorrhaphy. Clin J Pain. 2003 Jan-Feb;19(1):48-54. doi: 10.1097/00002508-200301000-00006. | |
| 38630543 |
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To protect personal health information IDP will not be shared.
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot_ICF | Yes | No | Yes | Study Protocol and Informed Consent Form | May 21, 2026 | Jun 24, 2026 | Prot_ICF_000.pdf |
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| ID | Term |
|---|---|
| D006552 | Hernia, Inguinal |
| ID | Term |
|---|---|
| D046449 | Hernia, Abdominal |
| D006547 | Hernia |
| D020763 | Pathological Conditions, Anatomical |
| D013568 | Pathological Conditions, Signs and Symptoms |
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| ID | Term |
|---|---|
| D012046 | Rehabilitation |
| ID | Term |
|---|---|
| D000359 | Aftercare |
| D003266 | Continuity of Patient Care |
| D005791 | Patient Care |
| D013812 | Therapeutics |
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2-arm parallel group randomized controlled trial
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The nature of this exercise-based intervention does not allow for masking.
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Measured by feedback forms during final data collection at 12 weeks post-op. |
| From enrollment to 12 weeks post-op |
| Background |
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| D006296 |
| Health Services |
| D005159 | Health Care Facilities Workforce and Services |