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Trial registered on ANZCTR
Registration number
ACTRN12617000716369
Ethics application status
Approved
Date submitted
2/05/2017
Date registered
17/05/2017
Date last updated
17/05/2017
Type of registration
Prospectively registered
Titles & IDs
Public title
Effect of detraining on physical condition and quality of life in elderly habitual exercisers
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Scientific title
Effect of detraining on physical condition, biochemical parameters and quality of life in elderly habitual exercisers
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Secondary ID [1]
291795
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none
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Universal Trial Number (UTN)
U1111-1196-0464
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Trial acronym
DETRex
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
frailty
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ageing
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Condition category
Condition code
Public Health
302487
302487
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0
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Health promotion/education
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Physical Medicine / Rehabilitation
302626
302626
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0
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Other physical medicine / rehabilitation
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Intervention/exposure
Study type
Observational
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Patient registry
False
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Target follow-up duration
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Target follow-up type
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Description of intervention(s) / exposure
All participants are finishing an exercise program which they have participated in for at least 9 months, and this study will assess their physical decline over three months following the end of the exercise program. Therefore, measurements will be performed twice: once at the end of the nine month exercise program and again 3 months later.
There will not be other measurements
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Intervention code [1]
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Not applicable
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Comparator / control treatment
No control group
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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Changes in strength of the upper extremity assessed by the handgrip strength measured by a Jamar dynamometer. Handgrip strength has been related to frailty and also sarcopenia.
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Assessment method [1]
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Timepoint [1]
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three months after the cessation of the exercise program, which is the detraining period
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Secondary outcome [1]
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quality of life using the SF-36 Quality of Life Questionnaire
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Assessment method [1]
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Timepoint [1]
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Measurements will be undertaken at the end of the exercise programe (baseline) and at 3 months after the cessation of the exercise program, i.e after the 3 months detarining period
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Secondary outcome [2]
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Change in cardiorrespiratory fitness by the 6 minute walk test measuring the distance covered in meters
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Assessment method [2]
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Timepoint [2]
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Measurements will be undertaken at the end of the exercise programe (baseline) and at 3 months after the cessation of the exercise program, i.e after the 3 months detraining period
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Secondary outcome [3]
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Number of falls by assessing the occurred during the 3 month period by self-report in a study diary
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Assessment method [3]
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Timepoint [3]
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The participants will record the number of falls ocurred during the three months of detraining,
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Secondary outcome [4]
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Change in the waist to hip ratio by measuring both the waist and the hip and calculating the ratio
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Assessment method [4]
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Timepoint [4]
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Measurements will be undertaken at the end of the exercise programe (baseline) and at 3 months after the cessation of the exercise program, i.e after the 3 months detraining period
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Secondary outcome [5]
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Changes in dynamic balance performing the “8-foot up and go” test
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Assessment method [5]
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Timepoint [5]
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Measurements will be undertaken at the end of the exercise programe (baseline) and at 3 months after the cessation of the exercise program, i.e after the 3 months detraining period
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Secondary outcome [6]
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changes in the strength of the upper extremity using the “arm curl” test (number of flexions and extensions of the arm within 30 s holding a hand dumbbell)
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Assessment method [6]
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Timepoint [6]
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Measurements will be undertaken at the end of the exercise programe (baseline) and at 3 months after the cessation of the exercise program, i.e after the 3 months detraining period
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Secondary outcome [7]
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changes in blood adiponectin measuring it from venous blood using ELISA technique
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Assessment method [7]
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Timepoint [7]
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Measurements will be undertaken at the end of the exercise programe (baseline) and at 3 months after the cessation of the exercise program, i.e after the 3 months detraining period
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Secondary outcome [8]
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changes in blood interleukin-6 measuring it from the blood using ELISA technique
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Assessment method [8]
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Timepoint [8]
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Measurements will be undertaken at the end of the exercise programe (baseline) and at 3 months after the cessation of the exercise program, i.e after the 3 months detraining period
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Secondary outcome [9]
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changes in blood C-reactive protein measuring it from the blood using ELISA technique
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Assessment method [9]
334403
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Timepoint [9]
334403
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Measurements will be undertaken at the end of the exercise programe (baseline) and at 3 months after the cessation of the exercise program, i.e after the 3 months detraining period
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Eligibility
Key inclusion criteria
The inclusion criteria will be to be enrolled in a supervised group exercise program for people aged over 65 during the previous 9 months, at least.
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Minimum age
65
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
-To have serious illnesses that prevents them to undertake physical exercise
-Participate in supervised exercise during the three months of detraining period
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Study design
Purpose
Natural history
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Duration
Longitudinal
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Selection
Defined population
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Timing
Prospective
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Statistical methods / analysis
Power and sample size
Sample size has been calculated to detect minimal significant effects on the variable of hand-grip strength, accepting a two-sided significance level of 0.05, a clinically relevant improvement of 2 kg in hand-grip strength and a standard deviation of 3 kg, and a power of 90%, 47 individuals are required. Presuming a drop-out of 5%, the resultant sample size is determinate in 50 individuals.
The IBM SPSS Statistics 22 statistical software package (SPSS, Inc., Chicago, IL) will be used to analyse the data. The normal distribution of the data will be evaluated using the Kolmogorov-Smirnov test. Continuous variables will be expressed as mean (SD) when normally distributed and as median with interquartile range (IQR) when not. Categorical variables will be expressed as frequency counts and percentages. To identify significant differences (with respect to baseline) in all variables after the 3 months of detraining, a paired Student’s-T test or a Wilcoxon test for dependent samples will be used.
Statistical significance will be set at p<0.05
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Recruitment
Recruitment status
Not yet recruiting
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Date of first participant enrolment
Anticipated
31/05/2017
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Actual
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
50
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Accrual to date
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Final
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Recruitment outside Australia
Country [1]
8852
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Spain
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State/province [1]
8852
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Bizkaia
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Funding & Sponsors
Funding source category [1]
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Government body
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Name [1]
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Basque Goverment
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Address [1]
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C/ Donostia-San Sebastian, 1
1010 Vitoria-Gasteiz
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Country [1]
296298
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Spain
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Primary sponsor type
Individual
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Name
Susana Gil
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Address
University of the Basque Country
Department of Physiology
Faculty of Medicine and Nursing
Barrio Sarriena s/n,
48940 Leioa,
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Country
Spain
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Secondary sponsor category [1]
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None
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Name [1]
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Address [1]
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Country [1]
295335
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Ethics Committee of the University of the Basque Country (UPV/EHU)
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Ethics committee address [1]
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Edificio de Rectorado Barrio sarriena Universidad del Pais Vasco/Euskal Herriko Unibertsitatea Leioa 48940 Bizakaia, Spain
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Ethics committee country [1]
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Spain
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Date submitted for ethics approval [1]
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16/11/2016
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Approval date [1]
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17/12/2016
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Ethics approval number [1]
297528
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M10_2015_204_GIL OROZKO
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Summary
Brief summary
The benefits effect of regular exercise has been well characterized. However, less attention has been given to the changes which occur following cessation of activity (detraining) particularly in the elderly. On many occasions, older adults who habitually attend exercise classes take extended holidays or have breaks and thus they interrupt their exercise. In these situations, it is not uncommon that they complain about stiffness of the joints, increased body pain and a decline in their well-being. Therefore, we hypothesize that old people that habitually exercise will suffer a decline in their physical condition and also their quality of life following the cessation of exercise. The main outcome will be the changes in the strength of the upper extremity measured with the hand-grip strength. Thus, the aim of the present study is to evaluate the effect of 3 months of detraining on different parameters of elderly people who have regularly exercised. In particular, we aim to characterize changes in the physical condition (strength, balance, cardiorespiratory fitness), health related quality of life, number of falls and biochemical parameters. In order to do that we will recruit a minimum of 50 participants from a supervised physical exercise program offered to people aged over 65 years in a public sports center in Getxo (Bizkaia, Basque Country). The inclusion criteria will be to be enrolled in a supervised group exercise program for people aged over 65 during the previous 9 months, at least. Measurements will be performed twice: once at the end of the nine month exercise program and again 3 months later, which is the detraining period. During detraining, participants will be asked to maintain their normal activities of daily living, and to abstain from participating in supervised exercise programs. The following measurements will be undertaken: -Age and gender -Number of falls which had occurred during the detraining period. -Anthropometric data: weight, height, circumference of the waist and hip, in order to calculate the body mass index and the waist-hip ratio calculated. -Health related quality of life using the SF-36 Quality of Life Questionnaire -6 minute walk test. The distance covered in 6 minutes will be measured (m) -Dynamic balance performing the “8-foot up and go” test -Strength of the upper extremity (hand-grip strength) using a hand dynamometry -Strength of the upper extremity using the “arm curl” test (number of flexions and extensions of the arm within 30 s holding a hand dumbbell) -Strength of the lower extremity using the “30 s chair stand ” -Blood adiponectin, interleukin-6 and C-reactive protein measuring it from the blood using ELISA technique
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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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Dr Susana Gil
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Address
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Department of Physiology
Faculty of Medicine and Nursing
University of the Basque Country (UPV/EHU)
Barrio Sarriena s/n
48940 Leioa
Bizkaia
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Country
74338
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Spain
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Phone
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+34 946012958
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Fax
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Email
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[email protected]
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Contact person for public queries
Name
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Susana Gil
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Address
74339
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Department of Physiology
Faculty of Medicine and Nursing
University of the Basque Country (UPV/EHU)
Barrio Sarriena s/n
48940 Leioa
Bizkaia
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Country
74339
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Spain
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Phone
74339
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+34 946012958
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Fax
74339
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Email
74339
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[email protected]
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Contact person for scientific queries
Name
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Susana Gil
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Address
74340
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Department of Physiology
Faculty of Medicine and Nursing
University of the Basque Country (UPV/EHU)
Barrio Sarriena s/n
48940 Leioa
Bizkaia
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Country
74340
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Spain
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Phone
74340
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+34 946012958
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Fax
74340
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Email
74340
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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
Type
Is Peer Reviewed?
DOI
Citations or Other Details
Attachment
Plain language summary
No
BACKGROUND: Little is known about the effects of ...
[
More Details
]
Study results article
Yes
Esain, I., Rodriguez-Larrad, A., Bidaurrazaga-Leto...
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Other files
No
Esain, I., Rodriguez-Larrad, A., Bidaurrazaga-Leto...
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Documents added automatically
Source
Title
Year of Publication
DOI
Embase
Health-related quality of life, handgrip strength and falls during detraining in elderly habitual exercisers.
2017
https://dx.doi.org/10.1186/s12955-017-0800-z
Embase
Exercise cessation in active older adults: Effects on inflammatory markers and adiponectin.
2020
https://dx.doi.org/10.1111/ggi.13907
N.B. These documents automatically identified may not have been verified by the study sponsor.
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