Targeted Prehabilitation With Physical Exercise and Inspiratory Muscle Training for Elderly Frail Patients Prior to Ventral Hernia Repair
试验速览
- 阶段
- 不适用
- 状态
- Enrolling By Invitation
- 入组人数
- 120
- 试验地点
- 1
- 主要终点
- Activity levels
研究概览
简要总结
The purpose of this study is to assess the physical fitness of patients undergoing hernia repair and correlate the postoperative outcomes and recovery as well as assess the impact of a targeted physical exercise program preoperatively in a cohort of frail, elderly patients.
The investigators hypothesize that physical exercise will improve activity levels in elderly patients with frailty prior to ventral hernia repair. The investigators further hypothesize that increased levels of activity preoperatively will correlate with improved postoperative outcomes.
详细描述
The goals of this study are to:
- assess the impact of a targeted physical exercise program on activity levels prior to ventral hernia repair in elderly, frail patients using wearable activity monitoring.
- correlate physical activity and the impact of physical exercise with postoperative outcomes, including quality of life, postoperative complications, length of hospital stay, discharge to home, and return to baseline activity.
The investigators intend to randomize one group of elderly, frail patients to perform an exercise program for 6-8 weeks prior to surgery and another group of elderly, frail patients to receive standard of care preoperative instructions.
The investigators will also collect data from a cohort of patients receiving a ventral or inguinal hernia repair who have a wearable activity monitor that are willing to download an application on their phone and allow us to monitor their activity levels prior to surgery.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 65 Years 至 —（Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Groups 1 & 2:
- •Age 65 or greater
- •Presence of a ventral hernia with plans for elective hernia repair with mesh
- •Willing to consent to study and randomization, including activity data capture
- •Score of ≥6 and ≤11 on the Edmonton Frail Scale OR 5-item modified Frail Index Score > 0
- •For patients with cardiac disease, additional referral for cardiac risk assessment may be performed at the discretion of the treating surgeon or anesthesiologist. If deemed appropriate risk, patients may still enroll.
- •Uses a smartphone that is capable of downloading the Health Kit application
- •Age 18 or older
- •Presence of a ventral hernia or inguinal hernia with plans for elective repair with mesh
- •Willing to consent to activity data capture
- •Uses a smartphone that is capable of downloading the Health Kit application
排除标准
- •Group 1 &2:
- •Unwilling or unable to consent to study or randomization
- •Joint or muscle pain with movement at a level of 5 out of 10 or higher per patient report
- •Score of ≥12 on Edmonton Frail Scale
- •mFI-5 positive for congestive heart failure (newly diagnosed or exacerbated within 30 days)
- •Functional dependence that prevents self-guided physical prehabilitation or other condition medically unsuitable for exercises (as determined by surgeon).
- •Parastomal hernia repair or repair without mesh
- •Plan for concurrent procedure
- •Unwilling or unable to consent to study
- •Joint or muscle pain with movement at a level of 5 out of 10 or higher per patient report
- •Parastomal hernia repair or repair without mesh
- •Plan for concurrent procedure
研究组 & 干预措施
Group 1 - Standard of Care
Patient receives standard of care instructions for preparing for ventral hernia repair surgery and recovery. Postoperative outcomes are measured.
干预措施: Standard of Care (SOC) (Other)
Group 3 - Observational Cohort
Patient's physical activity is monitored prior to receiving ventral or inguinal hernia repair surgery and postoperative outcomes are measured.
Group 2 - Physical Exercise Arm
Elderly patients with frailty participate in a 6-8 weeks of physical exercise program through the YMCA's SilverSneakers Program monitored by a wearable activity monitor. Patients will also complete respiratory training by using an incentive spirometer daily. Postoperative outcomes are measured
干预措施: Prehabilitation (Behavioral)
结局指标
主要结局
Activity levels
时间窗: 6-8 weeks preoperatively
Amount of time spent active measured by data from wearable activity monitors
次要结局
- Quality of Life Pre- and Postoperative Assessment(14-30 days postoperatively)
- Quality of Life Pre- and Postoperative Outcomes(14-30 days postoperatively)
- Postoperative Outcomes - Surgical Complications(14-30 days postoperatively)
- Postoperative Outcomes - Length of Stay(14-30 days postoperatively)
- Postoperative Outcomes - Discharge Location(14-30 days postoperatively)
- Postoperative Outcomes - Return to Baseline(14-30 days postoperatively)