AgeingACUSITNCT02605980
Acute Effects of Sitting Time in Older Adults
An observational study of Ageing, run by University of Birmingham at 1 site in United Kingdom.
Trial summary
United Kingdom (UK) physical activity guidelines for older people state that "All older adults should minimise the amount of time spent being sedentary (sitting) for extended periods" and "there is sufficient evidence to support a recommendation to reduce sedentary behaviour in older adults, but it is not currently… Read more about this study
- Who is it for?
- Ages 70 to 95 yearsHealthy volunteers can take part
- Conditions the study is for
- Ageing
- What is being tested?
- Sedentary time
- Type of treatment
- Lifestyle or therapy programme
- How many people
- 65 participants
- Where
- 1 siteUnited Kingdom
- Study dates
- 2 Mar 2016to 31 Dec 2018
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 70 to 95 years
- All sexes
- Healthy volunteers accepted
- Older adult
Study population: Community-dwelling healthy older adults aged 70 years or over. Must be ambulatory with or without a walking aid.
Who may be able to join
- 70 years or over
- Ambulatory with or without a walking aid.
Who cannot join
- History of myocardial infarction within previous 2 years
- Cardiac illness: moderate/ severe aortic stenosis, acute pericarditis, acute myocarditis, aneurysm, severe angina, clinically significant valvular disease, uncontrolled dysrhythmia, claudication within the previous 10 years
- Thrombophlebitis or pulmonary embolus within the previous 2 years
- History of cerebrovascular disease (CVA or TIA) within the previous 2 years
- Acute febrile illness within the previous 3 months
- Severe airflow obstruction
Show all 16Show fewer
- Uncontrolled metabolic disease (e.g., thyroid disease or cancer)
- Significant emotional distress, psychotic illness or depression within the previous 2 years
- Lower limb fracture sustained within the previous 2 years; upper limb fracture within the previous 6 months; non arthroscopic lower limb joint surgery within the previous 2 years
- Any reason for loss of mobility for greater than 1 week in the previous 2 months or greater than 2 weeks in the previous 6 months
- Poorly controlled atrial fibrillation
- Poor (chronic) pain control
- Resting systolic pressure >200 mmHg or resting diastolic pressure >100 mmHg
- Moderate/ severe cognitive impairment (MMSE <23)
- Impaired tissue viability (defined by a Waterlow risk assessment score >15).
- Based on Greig C.A. et al. Age Ageing 1994, 23: 185-9
Trial locations and contacts
1 site in 1 country.
About this study
Official title: The Acute Effects of Sitting Time on Physiological and Psychological Function in Older Adults
United Kingdom (UK) physical activity guidelines for older people state that "All older adults should minimise the amount of time spent being sedentary (sitting) for extended periods" and "there is sufficient evidence to support a recommendation to reduce sedentary behaviour in older adults, but it is not currently possible to suggest a specific time limit." The aim of this study is to identify key physiological and psychological outcomes influenced by acute periods of inactivity and what older people feel after these acute periods of inactivity. The investigators' main objective is to determine, through direct measurement and self report, the acute functional and cognitive effects of differing periods of sitting time. A secondary objective is to inform older people, professionals and organisations working with older people and policy makers on what duration of sedentary behaviour will lead to adverse outcomes in older people. The investigators will recruit ambulatory men and women aged 70 y and over who will be studied on three separate occasions, approximately one week apart to complete sedentary bouts of 1 h, 2 h and 4 h in a randomised crossover design. The investigators will explore the relationship between sitting time and changes in lower limb explosive power(primary outcome) measured before and after each bout. Secondary outcomes will include timed chair rise; Timed Up and Go; blood pressure; perception of musculoskeletal comfort/pain, vitality; mood and cognitive function. The investigators will also measure the stress hormone cortisol in samples of saliva taken at the start of the sitting session, 1 h, 2h and 4 h later. Characterising the acute effects of sitting time in older adults will enable the design of interventions to reduce sedentary time as well as inform professionals and policy makers on what duration of sedentary behaviour will lead to adverse outcomes.
Read the detailed description
Until relatively recently, sedentary behaviour was considered as the 'lower end' of the physical activity spectrum. However there is accumulating evidence from both epidemiological and observational studies which shows that sedentary behaviour per se rather than just low physical activity is also a major modifiable risk factor for chronic disease and predicts cardiovascular and all-cause mortality, independent of the amount of physical activity: A followup of the Australian Diabetic (AusDiab) cohort study showed a 46% increased risk of all-cause and an 80% increased risk of cardiovascular disease mortality in those watching four or more hours of television (TV) per day, compared with those watching TV for <2 h per day. In the Canadian Fitness Survey, a dose response relationship was shown between sitting time and cardiovascular disease and all-cause mortality. Significantly poorer long term mortality outcomes were found in those reporting spending most of the day sitting compared with those reporting less time sitting and this was consistent across all levels of self reported sitting time. Crucially, sitting time mortality relationships were apparent even among those who were physically active at other time points in their day. Although there is evidence supporting the longer term detrimental health effects of prolonged bouts of sedentary behaviour (sitting) across the age range, limited information exists with respect to the acute (or 'last bout') effects of sedentariness on the physiological and psychological health of older people.
Interestingly the current UK physical activity guidelines state that "while there is sufficient evidence to support a recommendation to reduce sedentary behaviour in older adults, it is not currently possible to suggest a specific time limit". There is the need to be able to characterise sitting time in older adults in terms of acute functional and cognitive effects, as well as identify the main effects that older people perceive as being important after periods of sitting. Thus there is a possibility of generating specific advice to older people, but this requires the elucidation of dose response relationships between sitting and health outcomes to be defined during carefully controlled studies. Although these studies have yet to be conducted, it is possible to select 'key' outcome measures based upon established evidence derived from epidemiological and smaller scale observational studies (viz recent studies reporting a significant negative association between sedentariness and physical and psychological impairment in older adults) as well as from other 'models' of physical inactivity such as bed rest and limb unloading. One such outcome is skeletal muscle power output. The ability to quickly produce sufficient muscle power is of paramount importance for controlling body movements during mobility related activities in older people, such as standing up from a chair or stair climbing. Muscle power output is therefore a functionally relevant outcome of the utmost importance to the maintenance of physical independence. In addition, older people are less able to maintain core temperature, partly due to a reduced muscle mass yet it is known that reducing muscle temperature by only 1˚C can result in a decline of power output of up to 26%. Work by the current study group has recently shown a reduction in muscle power (45%), sit to stand performance velocity (9%), gait speed and maximum quadriceps strength after only 45 minutes sitting in a cool environment (15 degrees Celsius). It is not known if sitting (and consequent muscle inactivity) in normal temperature environments leads to reduced power in older people. However, older people talk of more difficulty getting out of a chair when they have been sitting for long periods, so muscle power may be implicated. In older people with joint pain, the benefits of keeping moving and not just sitting are clear.
Although work on the effect of cold environments on cognition (dual task cost in walking speed and executive function using the trail making test) did not show any significant changes after 45 minutes exposure to 15 degrees Celsius in older people, little is known about effects on mood, well being or other cognitive and psychological outcomes of sitting. Associations between sitting and tiredness and depression have been shown in a longitudinal study of a middle aged Australian cohort in those who spent a total of >9 h/day sitting compared with those who spent <6 h/day sitting. However little is known about the effects of acute bouts of sitting. Although there is a body of evidence on the acute effects of physical activity, no published data reporting acute effects of sitting, or on dose response effects on psychological outcomes was found.
Thus, the current understanding of the acute effects of sitting time is severely limited. The proposed study will inform the development, implementation and evaluation of future interventions to reduce sedentary behaviour in older people by identifying key elements of the immediate (acute) benefits of breaking up long periods of sitting, aiding engagement with older adults about immediate individual level benefits of reduced sitting and identifying outcome measures sensitive to changes in sitting time. Alongside views of older people, it will provide practical messages that can ensure more effective take up of an intervention among older people and effective advice for the professionals that work with older people. For example, for professionals working in residential home settings or on hospital wards/ intermediate or transition care settings (post acute illness or surgery), the results of this research will give valuable information on desirable time periods for encouraging mobilisation.
- Conditions
- Ageing
- Being tested
- Sedentary time
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Sedentary timeBehavioural
| Study group | Role | What they receive |
|---|---|---|
| Male | Community-dwelling healthy older adults over the age of 70 years. Must be ambulatory, with or without walking aids Receives: Behavioral: Sedentary time | |
| Female | Community-dwelling healthy older adults over the age of 70 years. Must be ambulatory, with or without walking aids Receives: Behavioral: Sedentary time |
What is being measured
The primary outcome is the main question the study is designed to answer.
Change in lower limb extensor power (Nottingham Power Rig)
The design of the device includes an adjustable seat and a footplate connected through a chain and lever to a flywheel. There is an attached seat which is adjustable to the appropriate position for each participant, ensuring that when the footplate is fully depressed, the participant's leg will be in the extended position. The participant will sit upright in the seat with arms crossed across the chest and non- dominant leg resting with the foot flat on the floor or frame of the rig. The participants will be required to apply maximal force to the footplate, by extending their dominant leg with maximal effort. When force is applied to the footplate, the flywheel accelerates, initiating the data collection. The final velocity of the flywheel will be used to calculate power (W.kg-1), which will then be displayed on a computer interface.
Measured: This will be assessed seven times within a period of six weeks throughout the study. First will be at the start of study (first visit).Two more tests will be conducted each time on the second,third and final visits which will be one week apart.
Secondary outcomes (13)
Change in Timed chair rise (functional ability)
This is a measure of the time taken for each participant to rise from sitting on a chair to upright standing.
Measured: This will be assessed seven times across three sessions (one week apart) over a period of six weeks throughout the study i.e.at the start of study, and two more tests each time on the second,third and final visits.
Change in Timed Up and Go (marker of falls risk)
This test involves instructing the participants to stand from a seated position, walk forwards covering a marked out 3 meter distance, turn 360° around the 3 meter mark, walk back towards the chair and return to the seated position.
Measured: This measure will be assessed seven times across three sessions (one week apart) over a period of six weeks throughout the study period.
Change in blood pressure (postural hypotension)
Blood pressure will be measured using a fully digitalised blood pressure monitor in sitting and standing. The participants will be asked to remain relaxed with both feet flat on the floor. The blood pressure cuff will be applied around their right bicep, 2.5cm above the elbow joint. The digital screen will then display the systolic and diastolic blood pressure measurements for recording. Blood pressure measurements will be taken before the sitting bout, and after 1 hour, 2 hours and 4 hours.
Measured: Blood pressure will be recorded seven times across three sessions (one week apart) over a period of six weeks throughout the study period.
Change in balance (postural sway)
Postural sway will be assessed using a laser range finder with a 30cm range. The range finder will be attached to the participant when they rise from a chair after the sitting bouts to measure sway.
Measured: Postural sway as a measure of static balance will be assessed seven times across three sessions (one week apart) over a period of six weeks throughout the study.
Change in salivary cortisol
This is will be measured by providing a wad of cotton for participants to put in their mouth.
Measured: Salivary samples will be collected nine times across three sessions (one week apart) over a period of six weeks to measure cortisol levels in participants.
Change in serum inflammatory markers (Venepuncture)
Blood samples will be collected twice from participants on each of the three visits to measure inflammatory markers.
Measured: Serum inflammatory markers will be measured six times per participant across three sessions (one week apart) over a period of six weeks throughout the study.
Change in perception of musculoskeletal comfort
Participants will be asked to rate their level of pain following standing upright, specifically within their lower limb joints, on a scale of 0 (no pain) to 10 (agonising pain).
Measured: This will be assessed six times for each participant on three sessions (one week apart) over a period of six weeks throughout the study.
Change in subjective vitality scale
The Subjective Vitality Scale assesses psychological wellbeing in terms of the subjective feelings of being alive and full of energy, referred to as vitality (Ryan and Frederick, 1997).
Measured: Vitality will be assessed six times on three occasions (one week apart) over a six-week period throughout the study.
Change in Profile of Mood States (POMS)
The Brief Profile of Mood States (POMS) is a modified shorter version of the Profile of Mood States (McNair, Lorr \& Droppleman, 1989). This will be used in the present study as a measure of affective mood. Participants will be instructed to complete the task by rating the 30 mood states, on a scale of 1 (not at all) to 5 (extremely) based on their current mood.
Measured: Participants' mood will be assessed six times on three occasions (one week apart) over a six-week period throughout the study.The questionnaires will be administered before and after each of the three sitting sessions which will be about one week apart.
Change in simple reaction time (Simon Task)
This computer based test assesses cognitive function by creating stimulus- response conflict and measures the participant's capability to respond to the correct stimuli.
Measured: This test will be administered six times over a period of six weeks throughout the study. The test will be taken before and after each of the three sitting sessions which will be about one week apart.
Change in Digit Symbol Test score
This is a computer based measure of cognitive function. The test involves rows containing the symbols in a random order, with empty boxes displayed underneath the symbol. Using the digit-symbol look up table, the participant's task will be to complete the empty digit boxes to match the corresponding symbols, one at a time using the laptop keyboard.
Measured: This test will be taken six times over a period of six weeks throughout the study. The test will be taken twice (before and after 1 hour, 2 hours and 4 hours sitting sessions). The sessions will be about one-week apart.
Change in Trial Making Test B score
This cognitive test assesses executive function. It will be completed as a paper version of the Trail Making Test B. The participants will be instructed to complete the test by connecting the numbers and letters in an alternating numerical and alphabetical sequence, by drawing lines between the figures and alphabets (i.e. A, 1, B, 2, etc.) without removing the pen from the paper. Performance will be measured by the time taken to complete the test correctly, therefore the participants will be advised to complete the test as rapidly as possible.
Measured: Trial Making Test B will be administered six times over a period of six weeks throughout the study. The test will be administered before and after each of the three sitting sessions (1 hour, 2 hours and 4 hours). The sessions will be one week apart.
Change in Alice Heim 1&2 test (AH1,2)
Alice Heim 1 is the verbal reasoning part of the Alice Heim Group Ability Test (AH4). The section will be preceded by a short practice test . In the Alice Heim 2 test, participants will be instructed to select the most appropriate image based on the instructions given.This is the non-verbal reasoning part of the Alice Heim Group Ability Test (AH4).
Measured: AH1,2 will be administered six times over a six week period. The test will be taken before and after each of the three sitting sessions (1 hour, 2 hours and 4 hours). The sessions will be one week apart.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted17 Nov 2015 (estimated)
- Study start2 Mar 2016
- Primary completion26 Nov 2018
- Study completion31 Dec 2018
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for AgeingStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Cross-sectional
- Enrolment
- 65 participants (actual)
Sponsor and investigators
- Lead sponsor
- University of Birmingham
- Sponsor type
- University, hospital or other
- Collaborators
- The Dunhill Medical Trust, Glasgow Caledonian University
- Responsible party
- Sponsor
- Investigators
- Carolyn A Greig, PhD, Principal investigator, University of Birmingham
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02605980
- Sponsor's protocol ID
- 177149
- Acronym
- ACUSIT
- Status last verified
- Mar 2016
- First submitted
- 16 Oct 2015
- Last updated
- 11 Jun 2019
- Results posted
- No
- Data monitoring committee
- No
Study at a glance
From the registry record, last updated by the sponsor on 11 Jun 2019. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Acute Effects of Sitting Time on Physiological and Psychological Function in Older Adults
- ClinicalTrials.gov ID
- NCT02605980
- Acronym / sponsor ID
- ACUSIT / 177149
- Conditions
- Ageing
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 65 participants (actual)
- Lead sponsor
- University of BirminghamUniversity, hospital or other
- Collaborators
- The Dunhill Medical Trust, Glasgow Caledonian University
- Study start
- 2 Mar 2016 (actual)
- Primary completion
- 26 Nov 2018 (actual)
- Study completion
- 31 Dec 2018 (actual)
- First posted
- 17 Nov 2015 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
United Kingdom (UK) physical activity guidelines for older people state that "All older adults should minimise the amount of time spent being sedentary (sitting) for extended periods" and "there is sufficient evidence to support a recommendation to reduce sedentary behaviour in older adults, but it is not currently possible to suggest a specific time limit." The aim of this study is to identify key physiological and psychological outcomes influenced by acute periods of inactivity and what older people feel after these acute periods of inactivity. The investigators' main objective is to determine, through direct measurement and self report, the acute functional and cognitive effects of differing periods of sitting time. A secondary objective is to inform older people, professionals and organisations working with older people and policy makers on what duration of sedentary behaviour will lead to adverse outcomes in older people. The investigators will recruit ambulatory men and women aged 70 y and over who will be studied on three separate occasions, approximately one week apart to complete sedentary bouts of 1 h, 2 h and 4 h in a randomised crossover design. The investigators will explore the relationship between sitting time and changes in lower limb explosive power(primary outcome) measured before and after each bout. Secondary outcomes will include timed chair rise; Timed Up and Go; blood pressure; perception of musculoskeletal comfort/pain, vitality; mood and cognitive function. The investigators will also measure the stress hormone cortisol in samples of saliva taken at the start of the sitting session, 1 h, 2h and 4 h later. Characterising the acute effects of sitting time in older adults will enable the design of interventions to reduce sedentary time as well as inform professionals and policy makers on what duration of sedentary behaviour will lead to adverse outcomes.
Detailed description
Until relatively recently, sedentary behaviour was considered as the 'lower end' of the physical activity spectrum. However there is accumulating evidence from both epidemiological and observational studies which shows that sedentary behaviour per se rather than just low physical activity is also a major modifiable risk factor for chronic disease and predicts cardiovascular and all-cause mortality, independent of the amount of physical activity: A followup of the Australian Diabetic (AusDiab) cohort study showed a 46% increased risk of all-cause and an 80% increased risk of cardiovascular disease mortality in those watching four or more hours of television (TV) per day, compared with those watching TV for <2 h per day. In the Canadian Fitness Survey, a dose response relationship was shown between sitting time and cardiovascular disease and all-cause mortality. Significantly poorer long term mortality outcomes were found in those reporting spending most of the day sitting compared with those reporting less time sitting and this was consistent across all levels of self reported sitting time. Crucially, sitting time mortality relationships were apparent even among those who were physically active at other time points in their day. Although there is evidence supporting the longer term detrimental health effects of prolonged bouts of sedentary behaviour (sitting) across the age range, limited information exists with respect to the acute (or 'last bout') effects of sedentariness on the physiological and psychological health of older people.
Interestingly the current UK physical activity guidelines state that "while there is sufficient evidence to support a recommendation to reduce sedentary behaviour in older adults, it is not currently possible to suggest a specific time limit". There is the need to be able to characterise sitting time in older adults in terms of acute functional and cognitive effects, as well as identify the main effects that older people perceive as being important after periods of sitting. Thus there is a possibility of generating specific advice to older people, but this requires the elucidation of dose response relationships between sitting and health outcomes to be defined during carefully controlled studies. Although these studies have yet to be conducted, it is possible to select 'key' outcome measures based upon established evidence derived from epidemiological and smaller scale observational studies (viz recent studies reporting a significant negative association between sedentariness and physical and psychological impairment in older adults) as well as from other 'models' of physical inactivity such as bed rest and limb unloading. One such outcome is skeletal muscle power output. The ability to quickly produce sufficient muscle power is of paramount importance for controlling body movements during mobility related activities in older people, such as standing up from a chair or stair climbing. Muscle power output is therefore a functionally relevant outcome of the utmost importance to the maintenance of physical independence. In addition, older people are less able to maintain core temperature, partly due to a reduced muscle mass yet it is known that reducing muscle temperature by only 1˚C can result in a decline of power output of up to 26%. Work by the current study group has recently shown a reduction in muscle power (45%), sit to stand performance velocity (9%), gait speed and maximum quadriceps strength after only 45 minutes sitting in a cool environment (15 degrees Celsius). It is not known if sitting (and consequent muscle inactivity) in normal temperature environments leads to reduced power in older people. However, older people talk of more difficulty getting out of a chair when they have been sitting for long periods, so muscle power may be implicated. In older people with joint pain, the benefits of keeping moving and not just sitting are clear.
Although work on the effect of cold environments on cognition (dual task cost in walking speed and executive function using the trail making test) did not show any significant changes after 45 minutes exposure to 15 degrees Celsius in older people, little is known about effects on mood, well being or other cognitive and psychological outcomes of sitting. Associations between sitting and tiredness and depression have been shown in a longitudinal study of a middle aged Australian cohort in those who spent a total of >9 h/day sitting compared with those who spent <6 h/day sitting. However little is known about the effects of acute bouts of sitting. Although there is a body of evidence on the acute effects of physical activity, no published data reporting acute effects of sitting, or on dose response effects on psychological outcomes was found.
Thus, the current understanding of the acute effects of sitting time is severely limited. The proposed study will inform the development, implementation and evaluation of future interventions to reduce sedentary behaviour in older people by identifying key elements of the immediate (acute) benefits of breaking up long periods of sitting, aiding engagement with older adults about immediate individual level benefits of reduced sitting and identifying outcome measures sensitive to changes in sitting time. Alongside views of older people, it will provide practical messages that can ensure more effective take up of an intervention among older people and effective advice for the professionals that work with older people. For example, for professionals working in residential home settings or on hospital wards/ intermediate or transition care settings (post acute illness or surgery), the results of this research will give valuable information on desirable time periods for encouraging mobilisation.
Study design
- Observational model
- Cohort
- Time perspective
- Cross-sectional
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Male | – | Behavioral: Sedentary timeCommunity-dwelling healthy older adults over the age of 70 years. Must be ambulatory, with or without walking aids |
| Female | – | Behavioral: Sedentary timeCommunity-dwelling healthy older adults over the age of 70 years. Must be ambulatory, with or without walking aids |
Who may qualify
- Ages
- 70 to 95 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Older adult
- Study population
- Community-dwelling healthy older adults aged 70 years or over. Must be ambulatory with or without a walking aid.
Key inclusion criteria (2 listed)
- 70 years or over
- Ambulatory with or without a walking aid.
Key exclusion criteria (16 listed)
- History of myocardial infarction within previous 2 years
- Cardiac illness: moderate/ severe aortic stenosis, acute pericarditis, acute myocarditis, aneurysm, severe angina, clinically significant valvular disease, uncontrolled dysrhythmia, claudication within the previous 10 years
- Thrombophlebitis or pulmonary embolus within the previous 2 years
- History of cerebrovascular disease (CVA or TIA) within the previous 2 years
- Acute febrile illness within the previous 3 months
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Sedentary time | Behavioural | Female, Male |
Primary outcome
Change in lower limb extensor power (Nottingham Power Rig)
Time frame: This will be assessed seven times within a period of six weeks throughout the study. First will be at the start of study (first visit).Two more tests will be conducted each time on the second,third and final visits which will be one week apart.
The design of the device includes an adjustable seat and a footplate connected through a chain and lever to a flywheel. There is an attached seat which is adjustable to the appropriate position for each participant, ensuring that when the footplate is fully depressed, the participant's leg will be in the extended position. The participant will sit upright in the seat with arms crossed across the chest and non- dominant leg resting with the foot flat on the floor or frame of the rig. The participants will be required to apply maximal force to the footplate, by extending their dominant leg with maximal effort. When force is applied to the footplate, the flywheel accelerates, initiating the data collection. The final velocity of the flywheel will be used to calculate power (W.kg-1), which will then be displayed on a computer interface.
13 secondary outcomes
Change in Timed chair rise (functional ability)
Time frame: This will be assessed seven times across three sessions (one week apart) over a period of six weeks throughout the study i.e.at the start of study, and two more tests each time on the second,third and final visits.
Change in Timed Up and Go (marker of falls risk)
Time frame: This measure will be assessed seven times across three sessions (one week apart) over a period of six weeks throughout the study period.
Change in blood pressure (postural hypotension)
Time frame: Blood pressure will be recorded seven times across three sessions (one week apart) over a period of six weeks throughout the study period.
Change in balance (postural sway)
Time frame: Postural sway as a measure of static balance will be assessed seven times across three sessions (one week apart) over a period of six weeks throughout the study.
Change in salivary cortisol
Time frame: Salivary samples will be collected nine times across three sessions (one week apart) over a period of six weeks to measure cortisol levels in participants.
Change in serum inflammatory markers (Venepuncture)
Time frame: Serum inflammatory markers will be measured six times per participant across three sessions (one week apart) over a period of six weeks throughout the study.
Change in perception of musculoskeletal comfort
Time frame: This will be assessed six times for each participant on three sessions (one week apart) over a period of six weeks throughout the study.
Change in subjective vitality scale
Time frame: Vitality will be assessed six times on three occasions (one week apart) over a six-week period throughout the study.
Change in Profile of Mood States (POMS)
Time frame: Participants' mood will be assessed six times on three occasions (one week apart) over a six-week period throughout the study.The questionnaires will be administered before and after each of the three sitting sessions which will be about one week apart.
Change in simple reaction time (Simon Task)
Time frame: This test will be administered six times over a period of six weeks throughout the study. The test will be taken before and after each of the three sitting sessions which will be about one week apart.
Change in Digit Symbol Test score
Time frame: This test will be taken six times over a period of six weeks throughout the study. The test will be taken twice (before and after 1 hour, 2 hours and 4 hours sitting sessions). The sessions will be about one-week apart.
Change in Trial Making Test B score
Time frame: Trial Making Test B will be administered six times over a period of six weeks throughout the study. The test will be administered before and after each of the three sitting sessions (1 hour, 2 hours and 4 hours). The sessions will be one week apart.
Change in Alice Heim 1&2 test (AH1,2)
Time frame: AH1,2 will be administered six times over a six week period. The test will be taken before and after each of the three sitting sessions (1 hour, 2 hours and 4 hours). The sessions will be one week apart.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 11 Jun 2019.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Carolyn A Greig, PhD principal investigator
University of Birmingham
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Ageing, run by University of Birmingham at 1 site in United Kingdom.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 2 inclusion and 16 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 11 Jun 2019. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United Kingdom. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Change in lower limb extensor power (Nottingham Power Rig) (time frame: This will be assessed seven times within a period of six weeks throughout the study. First will be at the start of study (first visit).Two more tests will be conducted each time on the second,third and final visits which will be one week apart.). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 11 Jun 2019.