- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04999891
The Southeast and East Asian Post-Operative Delirium (SEAPOD) Study
The specific aim of the study will be to investigate the incidences and risk factors for postoperative delirium (POD) after hip fracture surgery in elderly patients aged ≥ 65 years in five different Southeast and East Asian countries.
The secondary objectives are outlined below:
- To investigate factors in the hospital environments, such as noise levels, ambient lighting, nursing ratios, ward bedding and climate control, that contribute to similarities and/or differences in POD occurrences in different countries and health systems
- To investigate patient factors, such as disease burden, mental health, education levels, and socioeconomic factors, that contribute to similarities and/or differences in POD occurrences in different countries and health systems
- To quantify the direct and indirect costs, as well as resource utilization, resulting from the development of POD in each country
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Hip fractures encompass all fractures of the upper (proximal) part of the thigh bone (femur). They are commonly divided into two types: intracapsular fractures, which represent those that occur within or proximal to the attachment of the hip joint capsule to the femur, and extracapsular, which represent fractures occurring below or distal to the attachment of the hip joint capsule.
Hip fractures are common in elderly people with an annual incidence rate estimated as 1.29/1000 person-years in men and 2.24/1000 person-years in women. It is the most common condition requiring physical rehabilitation in older adults. The majority (>95%) of people undergo hip surgery following hip fracture. The location of the fracture, stability, and degree of comminution (number of pieces the bone breaks into) determine which operative procedure should be used to repair the hip fracture. The aim of surgery, irrespective of the type of operation, is to reduce pain, facilitate early weight-bearing mobility to improve outcome, and facilitate independence in activities of daily living, such as bathing, dressing, and continence. However, hip fracture is associated with significant pain and loss of independence and function. Although 33-37% of patients return to their prior level of function within six months including those needing assistance, only 24% of people are independently mobile six months after hip fracture.
A major complication in elderly hip fracture patients is POD, with an incidence rate varying from 13% to 65%. POD after hip surgery was significantly associated with non-home discharge disposition, and higher odds of 30-day readmissions and 30-day mortality. POD is also associated with poor outcomes, such as lower rates of immediate postoperative weight bearing, increased pressure sores, and poorer recovery of activities of daily living. In addition, a recent meta-analysis showed that POD after hip surgery translates into long-term cognitive disease burden, by increasing the risk of incident dementia and cognitive decline by a marked odds ratio of 8.957.
No strong evidence exists regarding the treatment of delirium. Several studies performed on delirium prevention in hip fracture patients have described the use of care bundles such as orthogeriatric care and comprehensive geriatric care as an effective potential treatment for this patient group, although the evidence remains weak. However, Inouye et al stated that in the general geriatric population, 30% to 40% of the delirium episodes could be prevented by addressing modifiable risk factors.
Previous studies in the five Asian countries involved in this study show that the incidence of POD after hip fracture surgery varied greatly between countries and within countries: 12.8-27.9% in Japan, 5.07-51.3% in Korea, 13.4-45% in Thailand and 7.2% in Singapore. The incidence of POD in Malaysia can be estimated at 9-12% as reported in the recent HIP Attack trial. However, these studies were heterogenous in terms of patient selection, study methodology and hospital systems. These variations make it difficult to draw a direct comparison regarding the incidence of POD amongst Asian countries and to Western cohorts. Furthermore, the cost of POD to patients and institutions, both direct and indirect, is very poorly defined in Asian countries.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Locations
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Sendai, Japan
- Not yet recruiting
- Tohoku University School of Medicine
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Contact:
- Kotoe Kamata
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Tokyo, Japan
- Not yet recruiting
- Tokyo Women's Medical University
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Contact:
- Yasuko Nagasaka
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Seoul, Korea, Republic of
- Not yet recruiting
- Severance Hospital
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Contact:
- Jeong Min Kim
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Seoul, Korea, Republic of
- Not yet recruiting
- St Mary's Hospital
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Contact:
- Hyung Mook Lee
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Kuala Lumpur, Malaysia
- Not yet recruiting
- University of Malaya
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Contact:
- Pui San Loh
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Malaka, Malaysia
- Not yet recruiting
- Universiti Sains Malaysia
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Contact:
- Laila Ab Mukmin
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Singapore, Singapore, 169608
- Not yet recruiting
- Singapore General Hospital
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Contact:
- Sophia Tsong Huey Chew
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Singapore, Singapore
- Not yet recruiting
- Khoo Teck Puat Hospital
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Contact:
- Edwin Chuen Ping Seet
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Singapore, Singapore
- Recruiting
- National University Health System
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Singapore, Singapore
- Not yet recruiting
- Ng Teng Fong General Hospital
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Contact:
- Lyn Li Lean
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Singapore, Singapore
- Not yet recruiting
- Tan Tock Seng Hospital
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Contact:
- Vera Qinyi Lim
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Bangkok, Thailand
- Not yet recruiting
- Ramathibodi Hospital
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Contact:
- Varinee Lekprasert
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Bangkok, Thailand
- Not yet recruiting
- Siriraj Hospital
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Contact:
- Onuma Chaiwat
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Ability to provide informed consent
- Elderly patients aged 65 years and above
- Scheduled to undergo elective or emergency hip fracture surgery
Exclusion Criteria:
- History of psychiatric disease
- Baseline cognitive impairment or dementia (MOCA score < 24)
- Illiterate (unable to read or write with local language)
- Active history of substance abuse
- Has a second surgery planned within 5 days of index surgery
- Non-resident of Singapore
- Significant hearing and/or speech impairment
- Planned for admission into the intensive care unit after surgery
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
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Surgical Cohort
Elderly patients aged 65 and above who are planned for hip fracture surgery.
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Battery of neurocognitive tests and questionnaires including MoCA, PHQ-9, Falls History, FIFE, STOPBANG, Nutritional Survey, Global Physical Activity Questionnaire, Brief Pain Index, NuDESC, 3D-CAM.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Development of POD in elderly patients undergoing hip fracture surgery
Time Frame: Before surgery through to 1 year post surgery
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Collection of patient's demographics, medical records and surgical records to establish risk factors for POD development
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Before surgery through to 1 year post surgery
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Healthcare cost of POD in different countries and health systems
Time Frame: Before surgery through to study completion, an average of 1 year
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Quantify the direct and indirect costs, as well as resource utilization, resulting from the development of POD in each country by collecting hospitalization costs
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Before surgery through to study completion, an average of 1 year
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Similarities and/or differences in POD occurrences in different countries and health systems
Time Frame: Before surgery through to 1 year post surgery
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Collection of data such as noise levels, ambient lighting, nursing ratios, ward bedding and climate control, disease burden, mental health, education levels, and socioeconomic factors to establish similarities and/or differences in POD occurrences in different countries and health systems
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Before surgery through to 1 year post surgery
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Collaborators and Investigators
Investigators
- Principal Investigator: Lian Kah Ti, National University Health System
Publications and helpful links
General Publications
- Adams AL, Shi J, Takayanagi M, Dell RM, Funahashi TT, Jacobsen SJ. Ten-year hip fracture incidence rate trends in a large California population, 1997-2006. Osteoporos Int. 2013 Jan;24(1):373-6. doi: 10.1007/s00198-012-1938-5. Epub 2012 Feb 21.
- Lenze EJ, Skidmore ER, Dew MA, Butters MA, Rogers JC, Begley A, Reynolds CF 3rd, Munin MC. Does depression, apathy or cognitive impairment reduce the benefit of inpatient rehabilitation facilities for elderly hip fracture patients? Gen Hosp Psychiatry. 2007 Mar-Apr;29(2):141-6. doi: 10.1016/j.genhosppsych.2007.01.001.
- Uzoigwe CE, Burnand HG, Cheesman CL, Aghedo DO, Faizi M, Middleton RG. Early and ultra-early surgery in hip fracture patients improves survival. Injury. 2013 Jun;44(6):726-9. doi: 10.1016/j.injury.2012.08.025. Epub 2012 Sep 23.
- Handoll HH, Cameron ID, Mak JC, Finnegan TP. Multidisciplinary rehabilitation for older people with hip fractures. Cochrane Database Syst Rev. 2009 Oct 7;(4):CD007125. doi: 10.1002/14651858.CD007125.pub2.
- Morrison RS, Ahronheim JC, Morrison GR, Darling E, Baskin SA, Morris J, Choi C, Meier DE. Pain and discomfort associated with common hospital procedures and experiences. J Pain Symptom Manage. 1998 Feb;15(2):91-101.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2020/01350
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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