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An Interventional Study of Geriatric Frailty, Osteoporosis, and Depression

Primary Purpose

Frailty, Osteoporosis, Depression

Status
Completed
Phase
Not Applicable
Locations
Taiwan
Study Type
Interventional
Intervention
Exercise and nutritional integrated care
Usual care with education
Problem solving therapy (PST) integrated care
Sponsored by
National Health Research Institutes, Taiwan
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Frailty focused on measuring Frailty, Osteoporosis, Depression

Eligibility Criteria

65 Years - 79 Years (Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Scored 3-6 with the "Canadian Study of Health and Aging Clinical Frailty Scale (CSHA- CFS) Chinese Telephone Interview Version" (Telephone Interview Version is replaced by In-Person Interview Version in 2009 study)
  • Frailty index ≥ 1

Exclusion criteria:

  • Nursing home residents
  • Cannot speak any of the following three dialogues: Mandarin, Taiwanese and Haga
  • Hearing impairment interfering with communication or daily activities
  • Visual impairment interfering with communication or daily activities.
  • Cannot complete the screening instrument with the CSHA-CFS Chinese Telephone/In-Person Interview Version
  • Scored 1, 2, or 7 with the CSHA-CFS Chinese Telephone/In-Person Interview Version
  • Cognitive impairment defined as 3-item recall ≤ 1
  • Functional Impairment defined as not able to walk for 5 meters without assistance
  • Suicidal Ideation defined as Suicide Subscale of The Mini-International Neuropsychiatric Interview (M.I.N.I.) ≥ 6
  • Alcohol abuse disorders active within the last year. (score ≥ 2 on the CAGE)
  • Organic mental disorders (Seizure, brain tumor, brain surgeries), History of schizophrenia or bipolar diagnosed from psychiatrist

Sites / Locations

  • National Health Research Institutes

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Experimental

Experimental

Arm Label

UC group

ENIC group (IC group in 2009 study)

PSTIC group (IC group in 2009 study)

Arm Description

Usual care with education

Exercise and nutritional integrated care

Problem solving therapy integrated care

Outcomes

Primary Outcome Measures

improvement of frailty
Improvement of Cardiovascular Health Study Phenotypical Classification of Frailty (CHS_PCF) by at least one category (from pre-frail to robust, or from frail to pre-frail or robust) from baseline assessments.

Secondary Outcome Measures

Bone Mineral Density
Dual-emission X-ray absorptiometry (DXA) of both Hip and spine
quality of life assessment
EQ-5D index-Taiwan utility
QUALEFFO_31
pain, physical function,mental function
barthel index
PRIME-MD (only measured in pilot study)
The Primary Care Evaluation of Mental Disorders
BDI-II (only measured in 2009 study)
Beck Depression Inventory Second Edition
health-resource utilization
Original Frailty Indicators
Weight loss, Exhaustion, Low level physical activity, Slow walking speed, Weak grip strength
timed up and go
one leg stand time
dominant hand grip strength
dominant knee extension power
vitamin B12 in blood
vitamin D in blood
CRP in blood
testosterone in blood
IL-6 in blood

Full Information

First Posted
July 16, 2008
Last Updated
June 24, 2015
Sponsor
National Health Research Institutes, Taiwan
Collaborators
National Taiwan University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT00718432
Brief Title
An Interventional Study of Geriatric Frailty, Osteoporosis, and Depression
Official Title
Interventional Study of Geriatric Frailty, Osteoporosis, and Depression in a Community Based Randomized Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
June 2009
Overall Recruitment Status
Completed
Study Start Date
April 2008 (undefined)
Primary Completion Date
June 2010 (Actual)
Study Completion Date
December 2010 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
National Health Research Institutes, Taiwan
Collaborators
National Taiwan University Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Frailty, osteoporosis, and depression are three highly prevalent geriatric syndromes. Having these conditions are associated with adverse outcome in physical health, mental health, quality of life, and daily functioning. They are associated with higher mortality rates as well as increased health care cost. Risk factors, pathogenesis, clinical phenotypes, and interventions of these three geriatric syndromes are often related. Frailty is often defined as accumulations of multi-system deficiencies with increased vulnerability to multiple worse outcomes. Multifactorial, interdisciplinary integrated care models targeting frail older adults may have positive impacts on measurements associated with not only frailty, but also depression, or osteoporosis. The objective of this proposed study is to conduct a randomized control trial (RCT) to exam the effectiveness of integrated interventions on multiple outcomes among community-dwelling Taiwanese elders with high risks for frailty and/or osteoporosis, depression. We also plan to determine the differential effects of intervention between urban and rural area.
Detailed Description
This is a three-year study. In the first year, we conducted a pilot study to test the feasibility of implementing integrated model on frailty, osteoporosis, depression, and other outcomes. Another objective is to determine optimal sample size for next level intervention in year 2 and 3 (2009 study). Subjects are community-dwelling Taiwanese elders (65-79 years of age) living in Toufen Town in Miaoli County, Taiwan. Subjects are first screened with telephone interviews with the Chinese Canadian Study of Health and Aging _Clinical Frailty Scale (CCSHA_CFS). Eligible subjects are invited to a community hospital to be screened with the Health Study Phenotypic Classification of Frailty (CHS_PCF). Subjects scored ≥ 1 on the CHS_PCF are enrolled. With a 2 by 2 factorial design, subjects are first randomized into exercise/nutrition integrated care (ENIC) group and usual care (UC) group with education. Within each group, subjects are further randomized into problem solving therapy (PST) and usual care (UC) group with education by study care managers with pre-specified protocol. UC group subject received a study educational booklet with telephone follow up on compliance of booklet reading and suggested diet and exercise programs. Besides the booklets, ENIC group subjects received structured exercise 3 times/week with nutrition consultation as needed at hospital for 3 months while PST group subjects received 6 sessions of PST at hospital in 3 months. Subjects were followed at 3, 6 and 12 months. Primary outcome is improvement of the CHS_PCF by at least one category (from pre-frail to robust, or from frail to pre-frail or robust) from baseline analysis. Secondary outcomes include the physical function and performance, cognition, depression, quality of life, healthcare resource utilizations and bone-mineral density (BMD). Intention-to-treat analysis was applied. The pilot study enrolled 117 subjects, after analysis of the preliminary results, the study protocol for the second and third year (2009 study) is modified as follows: The study is conducted at one urban (Wanhua) and one rural (Toufen) site with roughly 150 participants at each site. Convenient samples referred from participant physicians' clinics instead of the population based samples in year 1 are used to decrease administration cost. Telephone based first stage screening instrument will be modified and validated for face to face interview. Longer intervention period (6-months) than year 1. Interventions provided in ENIC and PSTIC groups are combined into a single integrated care (IC) group. Interventions for IC group and UC group are minor changed, as described below. UC group: Inform the subjects about results of frailty, osteoporosis or depression assessment. The study educational booklet and CD-ROM on frailty, depression, osteoporosis, healthy diets, exercise protocols, and self-coping strategies will be given to participants. One 2-hour educational session is provided to participants to go through the booklet with demonstration of study exercise protocol. Subjects are encouraged to have balanced nutrition and regular exercises at home following the study protocol. Subjects were contacted bimonthly to check on how much they had read and watched the study material, and how well they had complied with the suggested diet and exercise protocols. However, it is at the subjects' discretion to discuss with their primary care physicians regarding the clinical interventions. IC group: Subjects will receive all interventions provided to the UC group. Furthermore, subjects will take exercise/rehabilitation courses at the participating hospitals twice a week for 24 weeks and 6 sessions of problem solving treatment (PST). If subjects do not improve on any of the 5 indicators from the (CHSPCF), comprehensive geriatric assessments (CGAs) are applied to identify more potential modifiable factors for frailty for individualized managements. Actual number of subjects enrolled in pilot study and 2009 study are 117 and 289 respectively and the total number of subjects enrolled in pilot study and 2009 study is 406.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Frailty, Osteoporosis, Depression
Keywords
Frailty, Osteoporosis, Depression

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
406 (Actual)

8. Arms, Groups, and Interventions

Arm Title
UC group
Arm Type
Active Comparator
Arm Description
Usual care with education
Arm Title
ENIC group (IC group in 2009 study)
Arm Type
Experimental
Arm Description
Exercise and nutritional integrated care
Arm Title
PSTIC group (IC group in 2009 study)
Arm Type
Experimental
Arm Description
Problem solving therapy integrated care
Intervention Type
Behavioral
Intervention Name(s)
Exercise and nutritional integrated care
Intervention Description
Besides the information sharing and the educational booklets, the ENIC group subjects are invited to take a structured exercise course at the participating hospital 3 times a week for 3 months. (twice a week for 24 weeks in 2009 study) The exercise program included warm up; a range of motion, stretching, and postural-correction activities; aerobic strengthening; balance; and cool down. The research team also inquired about the subjects' dietary compliance and responded to their dietary questions during the exercise sessions.
Intervention Type
Behavioral
Intervention Name(s)
Usual care with education
Intervention Description
The study educational booklet (plus CD-ROM in 2009 study) on frailty, depression, osteoporosis, healthy diets, exercise protocols, and coping strategies are given to the participants. UC group subjects will receive a 2-hour education based on the content of study booklet including 1-hour demonstration of study exercise program in 2009 study. Subjects are contacted monthly (bimonthly in 2009 study ) for frequencies of reading this booklet and the compliance on the suggested diet and exercise protocols. Subjects are also encouraged to follow with their primary care physicians for abnormal results identified from our assessments.
Intervention Type
Behavioral
Intervention Name(s)
Problem solving therapy (PST) integrated care
Intervention Description
Besides the information sharing and the educational booklets, the PSTIC group subjects will receive 6 sessions of PST (within 12 weeks in pilot study, within 24 weeks in 2009 study) aiming at solving the 'here-and-now' problems contributing to their mood-related condition and helps increase their self-efficacy. If major depressions are found, subjects are referred to their primary care physicians for further medical managements.
Primary Outcome Measure Information:
Title
improvement of frailty
Description
Improvement of Cardiovascular Health Study Phenotypical Classification of Frailty (CHS_PCF) by at least one category (from pre-frail to robust, or from frail to pre-frail or robust) from baseline assessments.
Time Frame
baseline, 3, 6, and 12 months
Secondary Outcome Measure Information:
Title
Bone Mineral Density
Description
Dual-emission X-ray absorptiometry (DXA) of both Hip and spine
Time Frame
baseline and 12 months
Title
quality of life assessment
Description
EQ-5D index-Taiwan utility
Time Frame
pilot study: baseline, 3, 6, and 12 months, 2009 study: baseline, 6, and 12 months
Title
QUALEFFO_31
Description
pain, physical function,mental function
Time Frame
pilot study: baseline, 3, 6, and 12 months, 2009 study: baseline, 6, and 12 months
Title
barthel index
Time Frame
pilot study: baseline, 3, 6, and 12 months, 2009 study: baseline and 12 months
Title
PRIME-MD (only measured in pilot study)
Description
The Primary Care Evaluation of Mental Disorders
Time Frame
baseline, 3, 6, and 12 months
Title
BDI-II (only measured in 2009 study)
Description
Beck Depression Inventory Second Edition
Time Frame
baseline, 6, and 12 months
Title
health-resource utilization
Time Frame
pilot study: baseline, 3, 6, and 12 months, 2009 study: baseline, 6, and 12 months
Title
Original Frailty Indicators
Description
Weight loss, Exhaustion, Low level physical activity, Slow walking speed, Weak grip strength
Time Frame
baseline, 3, 6, and 12 months
Title
timed up and go
Time Frame
baseline, 3, 6, and 12 months
Title
one leg stand time
Time Frame
baseline, 3, 6, and 12 months
Title
dominant hand grip strength
Time Frame
baseline, 3, 6, and 12 months
Title
dominant knee extension power
Time Frame
baseline, 3, 6, and 12 months
Title
vitamin B12 in blood
Time Frame
pilot study: baseline and 12 month, 2009 study: baseline and 6 months
Title
vitamin D in blood
Time Frame
pilot study: baseline and 12 month, 2009 study: baseline and 6 months
Title
CRP in blood
Time Frame
pilot study: baseline and 12 month, 2009 study: baseline and 6 months
Title
testosterone in blood
Time Frame
pilot study: baseline and 12 month, 2009 study: baseline and 6 months
Title
IL-6 in blood
Time Frame
pilot study: baseline and 12 month, 2009 study: baseline and 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
65 Years
Maximum Age & Unit of Time
79 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Scored 3-6 with the "Canadian Study of Health and Aging Clinical Frailty Scale (CSHA- CFS) Chinese Telephone Interview Version" (Telephone Interview Version is replaced by In-Person Interview Version in 2009 study) Frailty index ≥ 1 Exclusion criteria: Nursing home residents Cannot speak any of the following three dialogues: Mandarin, Taiwanese and Haga Hearing impairment interfering with communication or daily activities Visual impairment interfering with communication or daily activities. Cannot complete the screening instrument with the CSHA-CFS Chinese Telephone/In-Person Interview Version Scored 1, 2, or 7 with the CSHA-CFS Chinese Telephone/In-Person Interview Version Cognitive impairment defined as 3-item recall ≤ 1 Functional Impairment defined as not able to walk for 5 meters without assistance Suicidal Ideation defined as Suicide Subscale of The Mini-International Neuropsychiatric Interview (M.I.N.I.) ≥ 6 Alcohol abuse disorders active within the last year. (score ≥ 2 on the CAGE) Organic mental disorders (Seizure, brain tumor, brain surgeries), History of schizophrenia or bipolar diagnosed from psychiatrist
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ken N Kuo, M.D.
Organizational Affiliation
Natoinal Health Research Institutes
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Ching-Yu Chen, M.D.
Organizational Affiliation
Natoinal Health Research Institutes
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Rong-Sen Yang, M.D.
Organizational Affiliation
Natoinal Health Research Institutes
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Keh-Ming Lin, M.D.
Organizational Affiliation
Natoinal Health Research Institutes
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Chao Agnes Hsiung, M.D.
Organizational Affiliation
Natoinal Health Research Institutes
Official's Role
Principal Investigator
Facility Information:
Facility Name
National Health Research Institutes
City
Zhunan
Country
Taiwan

12. IPD Sharing Statement

Citations:
PubMed Identifier
23009149
Citation
Chan DC, Tsou HH, Yang RS, Tsauo JY, Chen CY, Hsiung CA, Kuo KN. A pilot randomized controlled trial to improve geriatric frailty. BMC Geriatr. 2012 Sep 25;12:58. doi: 10.1186/1471-2318-12-58.
Results Reference
derived

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An Interventional Study of Geriatric Frailty, Osteoporosis, and Depression

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