Activity Restrictions After Inguinal Hernia Repair

Sponsor
VA Eastern Colorado Health Care System (U.S. Fed)
Overall Status
Recruiting
CT.gov ID
NCT05867134
Collaborator
(none)
200
1
2
47
4.3

Study Details

Study Description

Brief Summary

This research is intended to be a pilot study to identify differences in outcomes for varied lifting and physical activity precautions following surgical repair of single-sided inguinal hernias. The researchers hypothesize that when given the autonomy to return to activity at the patient's discretion, convalescence will decrease in comparison to a control group given specific precautions to refrain from lifting and strenuous activity. Specific aims include differences in convalescence and surgical outcomes for each group, i.e. rates of complications, hernia recurrence, physical activity assessments pre and postop, and quality of life outcomes.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Removal of postoperative lifting restrictions
N/A

Detailed Description

This study will evaluate lifting restrictions in the postoperative period after inguinal hernia repair. Patients will be consented to the study via in person and electronic methods. Patients will be asked to answer a questionnaire regarding their current pre-operative activity levels in order to establish a baseline. Patients will undergo surgery according to normal medical recommendations and patient preference. Patients will be randomized into one of two groups: a control group told to practice standard of care at Eastern Colorado VA with return to activity precautions (6 weeks for open surgery, 2 weeks for minimally invasive surgery) and a treatment group told to "return to activity as tolerated/comfortable and stop activity if pain present". Patients will be observed in post-operative clinics and asked clinical questions, as well as questionnaires to assess their surgical experience, when they returned to activity, and overall quality of life. Medical charts will be reviewed in order to compare differences in responses and behaviors between the two groups and these data points will be recorded in a password protected document for data analysis.

This study aims to identify if lengthy recommendations for convalescence after inguinal hernia surgery are necessary and determine the impact of allowing the individual patient to have some autonomy in a recommendation to return to physical activity based on their own comfort level. This study could provide the surgical community with a more structured response after this common surgical procedure, as well as potentially reduce convalescence times for individual patients, leading to less economic burden on the individual and the community with returning to work precautions.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
200 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
Activity Restrictions After Inguinal Hernia Repair
Actual Study Start Date :
Jan 30, 2023
Anticipated Primary Completion Date :
Dec 31, 2024
Anticipated Study Completion Date :
Dec 31, 2026

Arms and Interventions

Arm Intervention/Treatment
Experimental: Activity as tolerated

Instruction will be a treatment group "return to activity as tolerated/comfortable and stop activity if pain present".

Behavioral: Removal of postoperative lifting restrictions
Patients will be randomized into one of two groups: a control group told to practice standard of care at Eastern Colorado VA with return to activity precautions (6 weeks for open surgery, 2 weeks for minimally invasive surgery) and a treatment group told to "return to activity as tolerated/comfortable and stop activity if pain present".

No Intervention: Standard Lifting Restrictions

Instructions will be "no lifting greater than 20lbs for 6 weeks for open surgery, 2 weeks for minimally invasive surgery".

Outcome Measures

Primary Outcome Measures

  1. Physiological parameter- Hernia recurrence [2 years]

    Study participants will be followed for 2 years following hernia surgery to evaluate for hernia recurrence in both study arms. Hernia recurrence would be determined by documentation in medical record by surgical teams.

  2. Physiological parameter- Postoperative Complications [2 months]

    Study participants will be evaluated after 2 months for incidence of postoperative complication due to hernia surgery. This includes seroma, hematoma, bleeding, surgical site infection, and wound dehiscence. This will be obtained from participant medical record as documented by clinical providers, primary care providers, surgery, and emergency medicine.

Secondary Outcome Measures

  1. Questionnaire- Postoperative Activity levels [6 weeks]

    Following surgery, study participants will follow specified activity restrictions (per study arm). At the 6 week mark after surgery, participants will complete a survey asking for quantification of vigorous, moderate, walking and sitting activities. Surveys include description of each activity.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 99 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Clinical diagnosis of unilateral inguinal hernia

  • Must be undergoing surgery

  • Must be able to consent

Exclusion Criteria:
  • Bilateral inguinal hernia

  • Recurrent inguinal hernia

  • Surgery scheduled with additional concomitant procedures

Contacts and Locations

Locations

Site City State Country Postal Code
1 Rocky Mountain Regional VA Medical Center Aurora Colorado United States 80045

Sponsors and Collaborators

  • VA Eastern Colorado Health Care System

Investigators

  • Principal Investigator: Edward Jones, VHAECH

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
VA Eastern Colorado Health Care System
ClinicalTrials.gov Identifier:
NCT05867134
Other Study ID Numbers:
  • 1610664
First Posted:
May 19, 2023
Last Update Posted:
May 19, 2023
Last Verified:
May 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by VA Eastern Colorado Health Care System
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 19, 2023