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STAND UP - Sedentary Behaviour in Older Adults: Investigating a New Therapeutic Paradigm

STAND UP - Sedentary Behaviour in Older Adults: Investigating a New Therapeutic Paradigm Work Package 3: Investigating the Effect of Sedentary Time, Reduced Sedentary Time and Increased Light-intensity Physical Activity on Metabolic and Psychological Health in Older Adults

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02453204
Acronym
STAND-UP
Enrollment
76
Registered
2015-05-25
Start date
2015-04-30
Completion date
2017-03-31
Last updated
2020-01-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Older Adults

Brief summary

Research has shown that reducing the time spent sitting can reduce the risk of many diseases, such as diabetes and heart disease, and improve health. It is estimated that many older adults typically spend 70% of their waking day sitting, but little is known about whether reducing sitting promotes health and well-being in this age group. The aim of this research is to investigate the health effects of reducing sitting time by replacing it with short periods of standing or walking in adults over the age of 65.

Interventions

BEHAVIORALSitting
BEHAVIORALStanding
BEHAVIORALWalking

Sponsors

University of Glasgow
CollaboratorOTHER
National Institute for Health Research, United Kingdom
CollaboratorOTHER_GOV
National Health Service, United Kingdom
CollaboratorOTHER_GOV
University of Leicester
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
65 Years to 79 Years
Healthy volunteers
Yes

Inclusion criteria

* Adults aged between 65 to 79 years inclusive * Able to walk (without any assistive devices and not requiring assistance from another person) * Ability to communicate in and understand English to participate in the informed consent process.

Exclusion criteria

* Regular purposeful exercise (≥75 minutes of self-reported vigorous exercise per week) * Inability to stand or undertake light ambulation * Psychological condition which limits participation in the study (e.g. dementia) * Inability to communicate or understand English * Steroid use * Use of glucose lowering medication * Inability to give informed consent

Design outcomes

Primary

MeasureTime frameDescription
Insulin area under the curve3 experimental intervention study visits over an estimated period of 1 monthSamples will be batched and analysed at the end of the study within a certified research laboratory at the Institute of Cardiovascular and Medical Sciences (ICAMS), University of Glasgow. Samples collected at the Leicester Diabetes Centre will be sent by courier in specialist containers and packed with dry ice.

Secondary

MeasureTime frameDescription
Glucose area under the curve3 experimental intervention study visits over an estimated period of 1 month
Triglyceride area under the curve3 experimental intervention study visits over an estimated period of 1 month
1H NMR Metabolomics spectroscopy3 experimental intervention study visits over an estimated period of 1 monthHydrogen-1 Nuclear Magnetic Resonance assessment undertaken on blood samples collected throughout experimental intervention days
Blood pressure3 experimental intervention study visits over an estimated period of 1 month
Felt Arousal Scale (0-5)3 experimental intervention study visits over an estimated period of 1 monthPositive affect and mood measured using the 6-point Likert Felt Arousal scale (0 = low arousal to 5 = high arousal) that will be used to assess arousal.
Feeling Scale (-5 to +5)3 experimental intervention study visits over an estimated period of 1 monthPositive affect and mood measured using the 11-point Likert Feeling Scale (-5 = very bad to +5 = very good) will be used to assess affective valence.
Semantic Verbal Fluency Test (number of items)3 experimental intervention study visits over an estimated period of 1 monthThe Semantic Verbal Fluency Test assesses semantic memory and language, and participants will be asked to name as many items as they can that belong to a particular category. The categories selected for each of the experimental days will be clothing and animals.
Hopkins Verbal Learning Test (number of words recalled)3 experimental intervention study visits over an estimated period of 1 monthThe Hopkins Verbal Learning Test assesses verbal learning and working memory and requires immediate and delayed recall of a series of 12 words over three learning trials. Participants will be requested to undertake the delayed recall component at the end of the first set of cognitive function tests and during the second set of cognitive function tests on experimental intervention days.
Trail Making Tests A (time to complete)3 experimental intervention study visits over an estimated period of 1 monthThe Trail Making Tests A assesses cognitive flexibility and requires connecting randomly located numbers in numerical order (e.g. 1,2,3,4).
Trail Making Tests B (time to complete)3 experimental intervention study visits over an estimated period of 1 monthThe Trail Making Tests B assesses cognitive flexibility and requires connecting randomly located numbers and letters in numerical and alphabetical order alternately (e.g. 1,A,2,B,3,C).
Rapid Visual Information Processing Test (number of sequences detected and errors)3 experimental intervention study visits over an estimated period of 1 monthThe Rapid Visual Information Processing Test assesses sustained visual attention using numbers and requires both selective attention and working memory. This test displays a number on screen that changes between odd and even digits and individuals must detect target sequences of three odd or three even consecutive digits.
Karolinska Sleepiness Scale (1-9)3 experimental intervention study visits over an estimated period of 1 monthSleep quality measured using the 9-point Likert Karolinska Sleepiness Scale (1= very alert to 9= very sleepy, fighting sleep, an effort to keep awake) based on a self-reported subjective assessment of the participant's level of drowsiness at the time.

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 23, 2026