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Trial registered on ANZCTR
Registration number
ACTRN12617001628336
Ethics application status
Approved
Date submitted
27/11/2017
Date registered
13/12/2017
Date last updated
13/12/2017
Type of registration
Retrospectively registered
Titles & IDs
Public title
Effectiveness of a combination of Tai Chi plus Thera-bands on stress, depression, anxiety, pain, ans well-being in older sedentary office workers: a pilot randomized controlled trial
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Scientific title
Effectiveness of a combination of Tai Chi plus Thera-bands on stress, depression, anxiety, pain, ans well-being in older sedentary office workers: a pilot randomized controlled trial
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Secondary ID [1]
293460
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None
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
stress
305641
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depression
305643
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anxiety
305644
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pain
305645
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Falls
305769
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Condition category
Condition code
Public Health
304869
304869
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0
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Health promotion/education
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Mental Health
304992
304992
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0
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Anxiety
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Mental Health
304993
304993
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0
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Depression
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Intervention group used Tai Chi combined with resistance training (i.e. Thera-band resistance training). The first 10 forms of the Yang style Tai Chi was used. Participants practiced Tai Chi while holding a Thera-band by both hands three time per week for 12 weeks plus a 2-week learning stage. Each session lasted for 45 minutes, including 10-minute warm up, 30-minute Tai Chi plus Thera-band exercise, and 5-minutes cool down. The resistance training was performed using Thera-Band®, The Hygenic Corporation, Akron, OH, USA.
One professional Tai Chi teacher conducted the sessions, each session had a minimum 1 person, and maximum 5 person. The intervention was undertaken in Griffith University, QLD, Australia (Nathan campus, Mount Gravatt campus, and Gold Coast campus). Sessions were conducted in the seminar rooms in these three campuses of Griffith University. Tai Chi and resistance training were administered during the same sessions. Attendance rate was recorded by signing participants' names on the attendance table of each session. Class capacity was also recorded.
Resistance training was used in conformed to the guideline of physical activity recommended for the elderly. Participants used the low resistance intensity at learning stage, and then adjusted to the higher intensity every fortnight if participants reported their rating of perceived exertion (RPE) at a level below five on the RPE scale during the intervention. Exercise intensity was progressively increased by adjusting the width of grip (based on the Thera-Band® force-elongation table) or adapting the resistance of the Thera-bands from tan to yellow and further to black.
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Intervention code [1]
299702
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Treatment: Other
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Comparator / control treatment
Control group used Tai Chi exercise (i.e. the first 10 forms of Yang style Tai Chi)
The first 10 forms of the Yang style Tai Chi was used. Participants practiced Tai Chi three time per week for 12 week splus a 2-week learning stage. Each session lasted for 45 minutes, including 10-minute warm up, 30-minute Tai Chi exercise, and 5-minutes cool down.
One professional Tai Chi teacher conducted the sessions, each session had a minimum 1 person, and maximum 5 person. The intervention was undertaken in Griffith University, QLD, Australia (Nathan campus, Mount Gravatt campus, and Gold Coast campus). Sessions were conducted in the seminar rooms in these three campuses of Griffith University. Attendance rate was recorded by signing participants' names on the attendance table of each session. Class capacity was also recorded each session.
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Control group
Active
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Outcomes
Primary outcome [1]
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Stress (Perceived Stress Scale)
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Assessment method [1]
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Timepoint [1]
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Baseline, 6 weeks, and 12 weeks after intervention commencement
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Primary outcome [2]
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Depression (Centre for Epidemiological Studies Depression Scale version 10)
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Assessment method [2]
304063
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Timepoint [2]
304063
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Baseline, 6 weeks, and 12 weeks after intervention commencement
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Primary outcome [3]
304159
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Anxiety (Geriatric Anxiety Inventory)
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Assessment method [3]
304159
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Timepoint [3]
304159
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Baseline, 6 weeks, and 12 weeks after intervention commencement
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Secondary outcome [1]
340817
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Pain (Visual Analogue Scale), this outcome is primary.
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Assessment method [1]
340817
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Timepoint [1]
340817
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Baseline, 6 weeks, and 12 weeks after intervention commencement
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Secondary outcome [2]
341113
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Lower body strength (30-second chair stand test), this outcome is primary
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Assessment method [2]
341113
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Timepoint [2]
341113
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Baseline, 6 weeks, and 12 weeks after intervention commencement
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Secondary outcome [3]
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Arm strength (Grip strength test), this outcome is primary
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Assessment method [3]
341114
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Timepoint [3]
341114
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Baseline, 6 weeks, and 12 weeks after intervention commencement
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Secondary outcome [4]
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Balance (Functional reach test), this outcome is primary.
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Assessment method [4]
341115
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Timepoint [4]
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Baseline, 6 weeks, and 12 weeks after intervention commencement
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Secondary outcome [5]
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Endurance (2-minute walk test), this outcome is primary
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Assessment method [5]
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Timepoint [5]
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Baseline, 6 weeks, and 12 weeks after intervention commencement
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Secondary outcome [6]
341117
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The feasibility of this study, which included percentage of recruitment, intervention acceptability, participant retention, data missing, adherence, and intervention fidelity, theses are also primary
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Assessment method [6]
341117
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Timepoint [6]
341117
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After the intervention
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Eligibility
Key inclusion criteria
1. office workers (administtrative and academic staff) aged 55 years and over
2. Independently ambulant
3. Engaging in less than 60 minutes of accumulated moderate intensity physical activity (e.g. brisk walking, bicycling, Yoga) per week
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Minimum age
55
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
Yes
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Key exclusion criteria
1. Serious health issues that prevent you becoming more physically active (measured by the Physical Activity Readiness Questionnaire)
2. Significant vision impairment (not able to see and follow instruction)
3. Tai Chi experience in the past one year (obtaining Tai Chi exercise for any reason)
4. Cannot endure Tai Chi exercise (moderate intensity activity) for 45 minutes three times per week
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Sealed envelopes were used to randomize participants to either the intervention or the control group.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
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Who is / are masked / blinded?
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Intervention assignment
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Other design features
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Phase
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Type of endpoint/s
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Statistical methods / analysis
A total of 40 participants (i.e. 20 participants in each group) will be recruited. This proposed sample size is considered adequate for a pilot RCT study for standardised effect sizes that range from small to medium
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
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Actual
23/01/2017
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Date of last participant enrolment
Anticipated
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Actual
28/06/2017
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Date of last data collection
Anticipated
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Actual
5/10/2017
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Sample size
Target
40
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Accrual to date
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Final
40
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Recruitment in Australia
Recruitment state(s)
QLD
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Funding & Sponsors
Funding source category [1]
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University
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Name [1]
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Griffith University HDR financial support
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Address [1]
298084
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Room 8.56, Gold Coast campus, Griffith University Qld 4222
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Country [1]
298084
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Australia
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Primary sponsor type
University
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Name
Griffith University
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Address
Nathan campus Griffith University, 170 Kessels Road, NATHAN QLD 4111
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Country
Australia
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Secondary sponsor category [1]
297163
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None
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Name [1]
297163
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Address [1]
297163
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Country [1]
297163
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
299107
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Griffith University Human Research Ethics
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Ethics committee address [1]
299107
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Level 0, Bray Centre (N54), Griffith University, 170 Kessels Road, Nathan Qld 4111
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Ethics committee country [1]
299107
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Australia
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Date submitted for ethics approval [1]
299107
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08/11/2016
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Approval date [1]
299107
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22/11/2016
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Ethics approval number [1]
299107
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Griffith University Reference Number: 2016/872
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Summary
Brief summary
This study was to compare the effectiveness of a combination of Tai Chi plus Thera-bands on both mental health and physical futbess with Tai Chi exercise only in older sedentary office workers; and to examine the feasibility of, and to support refinement of, the protocol, methods, and procedure. The study hypothesis that Tai Chi plus thera-bands exercise could effectively improve levels of stress, depression, anxiety, and pain, as well as physical fitness.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Prof Wendy Moyle
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Address
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Menzies Health Institute Queensland, Nathan campus, Griffith University, 170 Kessels Road QLD 4111, Australia
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Country
79310
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Australia
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Phone
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+61 (07) 373 55526
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Fax
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Email
79310
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[email protected]
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Contact person for public queries
Name
79311
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Meiling Qi
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Address
79311
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School of Nursing and Midwifery, Health Science, N48, Nathan campus, Griffith University, 170 Kessels Road QLD 4111, Australia
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Country
79311
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Australia
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Phone
79311
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+61 449895159
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Fax
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Email
79311
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[email protected]
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Contact person for scientific queries
Name
79312
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Meiling Qi
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Address
79312
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School of Nursing and Midwifery, Health Science, N48, Nathan campus, Griffith University, 170 Kessels Road QLD 4111, Australia
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Country
79312
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Australia
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Phone
79312
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+61 449895159
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Fax
79312
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Email
79312
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[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
Source
Title
Year of Publication
DOI
Embase
Effects of Tai Chi Combined with Theraband Training on Physical Fitness, Psychological Well-being, and Pain in Older Sedentary Office Workers: A Pilot Randomized Controlled Trial.
2019
https://dx.doi.org/10.1097/TGR.0000000000000244
N.B. These documents automatically identified may not have been verified by the study sponsor.
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