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RecruitingNCT05468255Updated Apr 10, 2024

The Impact of Removal of Exercise on Glycemic Control and Vascular Health in Older Active Adults

An interventional study of removal of exercise in Glucose Intolerance, Exercise and Vascular Function, sponsored by Old Dominion University. Recruiting at 1 site in United States. Per ClinicalTrials.gov, last updated 2024-04-10.

Sponsored by Old Dominion University · Not applicable, Interventional, and Basic science

From the registry’s dates

  • Primary completion was expected by Jan 2025, 1 year 9 months ago, but the record still lists the study as recruiting.
  • Started Jul 2022; still recruiting 4 years 3 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
40
Allocation
Randomized
Sex
All
01

Study summary

The purpose of this study is to determine if an acute bout of removal of exercise reduces enothelial function and glycemic control in an active, older adult population; and whether a 3 day return to exercise restores this response. Glycemic control is the blood glucose response following the consumption of a meal. It is an indicator of insulin resistance (or type 2 diabetes) and impaired glycemic control has been suggested to lead to cardiovascular disease. Endothelial function has been shown to be improved by chronic or acute increases in physical activity. Both of these have been shown to be impaired to acute bouts of inactivity in young populations; however the impact of acute inactivity in older adults is less understood. In this proposal the investigators will examine 1)how quickly impairments in glycemic control occur to acute physical inactivity in older adults who exercise, 2) how quickly impairments in endothelial function occur to acute inactivity in older adults who exercise, and 3) whether 3 days of a return to exercise restores these responses.

02

Conditions studied

  • Glucose Intolerance
  • Exercise
  • Vascular Function
03

In context

Glucose Intolerance

793 studies on the registry are indexed under Glucose Intolerance; 115 are open to participants now.

This study's planned enrollment of 40 is below the median of 56 across 661 interventional studies indexed under Glucose Intolerance.

Browse Glucose Intolerance studies →

Lead sponsor

Old Dominion University is the lead sponsor of 27 studies on the registry; 4 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. 55 years and older, 18-40 years old
  2. Healthy, physically active, performing at least 90 min/week of physical activity
  3. Free of physical limitations that may interfere with alterations in daily physical activity levels

Exclusion criteria

Exclusion Criteria:

  1. Physician diagnosed , hepatitis, or tuberculosis.
  2. Body weight change of greater than 5% within the previous 2 months
  3. Smoking within the previous 2 months.
  4. Taking medications that alter blood glucose levels
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

HIV

The human immunodeficiency virus, which weakens the immune system.

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05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Crossover assignment
Masking
None (open label)
Enrollment
40 participants (estimated)

Study arms

  • Experimental
    Metabolic

    Metabolic: Participants will have their blood glucose levels measured via continuous glucose monitoring for 3 days while participating in their normal exercise routines (EX). Participants will also have their blood glucose levels measured for 3 days while not exercising (NOEX), following immediately by 3 days of a return to normal activity(REX). Participants will be randomized to participate in the EX or NOEX/REX phases first. The EX and NOEX/REX phases will be separated by at least 1 week

    Other: removal of exercise

  • Experimental
    Vascular

    Vascular: Participants will have their blood vessel health measured while performing their normal exercise routines (EX) and while undergoing 1, 3, 5 days of no exercise (NOEX) followed immediately by 1 and 3 days of return to exercise (REX).

    Other: removal of exercise

Interventions

  • Otherremoval of exercise

    Subjects will stop doing their normal exercise routines for 3 or 5 days and then subjects will resume doing their normal exercise routines for 3 days.

    Also known as: return to exercise

06

What researchers measure

Primary outcomes

  1. Continuous glucose monitoring

    Time frame: 3 days before removal of exercise

  2. Continuous glucose monitoring

    Time frame: After removal of exercise for 5 days

  3. Continuous glucose monitoring

    Time frame: After return to exercise for 3 days

  4. Flow mediated dilation

    This measure assess blood vessel health non-invasively

    Time frame: 3 days before removal of exercise

  5. Flow mediated dilation (vascular health)

    This measure assess blood vessel health non-invasively

    Time frame: After removal of exercise for 5 days

  6. Flow mediated dilation (vascular health)

    This measure assess blood vessel health non-invasively

    Time frame: After return to exercise for 3 days

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 10, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05468255
Lead sponsor
Old Dominion University
Responsible party
Leryn Reynolds (Assistant Professor, Old Dominion University) — Principal investigator
First posted
Jul 21, 2022
Start date
Jul 25, 2022
Primary completion
Jan 30, 2025 (estimated)
Completion
Apr 1, 2025 (estimated)
Last update
Apr 10, 2024

Study contacts

Leryn Reynolds
Contact
lreynold@odu.edu
757-683-4974

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
Yes
View the source record on ClinicalTrials.gov ↗

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