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Health Effects of Reducing Sedentary Behavior

Health Effects of Reducing Sedentary Behavior

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03609255
Enrollment
21
Registered
2018-08-01
Start date
2018-08-13
Completion date
2018-10-08
Last updated
2018-10-24

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

Conditions

General Population

Brief summary

A recent review indicated that sedentary behavior has been associated with increased morbidity and mortality but the intervention studies frequently focus only on changing sedentary behavior (reducing sedentary time) without measuring health-associated outcomes. Elevated cortisol (related to stress) has been linked with health risks. Improved physical fitness has been linked with improved cortisol responses to psychosocial stressors. In addition, increased physical activity induced favorable effects upon low density lipoprotein, high density lipoprotein, and total cholesterol. Previous study also indicated that increasing daily steps have positive effect on blood glucose in people with impaired glucose tolerance. Ultimately, the investigators think that sedentary intervention and stress management may have benefits on these health indicators. As such the investigators will examine whether sedentary intervention or stress management can have positive effect on human health by measuring salivary cortisol, blood lipid profile, fasting blood glucose, blood pressure, resting energy expenditure, and body composition.

Interventions

Educational handouts for sedentary behavior and strategies reducing sedentary behavior and weekly videos related to reduced sedentary behavior

BEHAVIORALReducing stress

Educational handouts for sedentary behavior and stress management handout and weekly videos related stress management

BEHAVIORALControl

An educational handout for sedentary behavior and weekly neutral topic videos

Sponsors

Texas Tech University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

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

Inclusion criteria

* Age: 18-65 years.

Exclusion criteria

* Unable/unwilling to provide informed consent. * Having mobility impairment. * Current severe untreated depression (i.e., score in the severe depression range on the Hospital Anxiety and Depression Scale; HADS). * Women who are pregnant or nursing. * Currently smoking (within last 12 months). * Currently use medications that affect salivary cortisol level (i.e. prednisone, dexamethasone). * Have been diagnosed Addison's disease.

Design outcomes

Primary

MeasureTime frameDescription
Daily stepsBaseline (pre-intervention) and 4 weeks (post-intervention)Changes in daily steps measured via pedometer.
Stress improvement in sedentary behavior group (SB)Baseline (pre-intervention) and 4 weeks (post-intervention)Improvement in stress as measured via Perceived Stress Scale (PSS) in SB.
Stress improvement in stress management group (SR)Baseline (pre-intervention) and 4 weeks (post-intervention)Improvement in stress as measured via Perceived Stress Scale (PSS) in SR.
Compare the changes of stress levels between SB and SRBaseline (pre-intervention) and 4 weeks (post-intervention)Compare the changes of stress levels as measured via Perceived Stress Scale (PSS) between SB and SR.

Secondary

MeasureTime frameDescription
Compared the changes in TC between SB and SRBaseline (pre-intervention) and 4 weeks (post-intervention)Compared the changes in TC between SB and SR.
Compared the changes in TG between SB and SRBaseline (pre-intervention) and 4 weeks (post-intervention)Compared the changes in TG between SB and SR.
Changes in low density lipoprotein (LDL) in SBBaseline (pre-intervention) and 4 weeks (post-intervention)Changes in LDL as measured via finger stick in SB.
Changes in high density lipoprotein (HDL) in SBBaseline (pre-intervention) and 4 weeks (post-intervention)Changes in HDL as measured via finger stick in SB.
Changes in total cholesterol (TC) in SBBaseline (pre-intervention) and 4 weeks (post-intervention)Changes in TC as measured via finger stick in SB.
Changes in triglyceride (TG) in SBBaseline (pre-intervention) and 4 weeks (post-intervention)Changes in TG as measured via finger stick in SB.
Changes in fasting blood glucose in SBBaseline (pre-intervention) and 4 weeks (post-intervention)Changes in fasting blood glucose as measured via finger stick in SB.
Changes in body fat in SBBaseline (pre-intervention) and 4 weeks (post-intervention)Changes in body fat as measured via BODPOD in SB.
Changes in weight in SBBaseline (pre-intervention) and 4 weeks (post-intervention)Changes in weight as measured via BODPOD in SB.
Changes in blood pressure in SBBaseline (pre-intervention) and 4 weeks (post-intervention)Changes in blood pressure as measured via Omron Digital BP Monitor HEM-907XL in SB.
Changes in low density lipoprotein (LDL) in SRBaseline (pre-intervention) and 4 weeks (post-intervention)Changes in LDL as measured via finger stick in SR.
Compared the changes in fasting blood glucose between SB and SRBaseline (pre-intervention) and 4 weeks (post-intervention)Compared the changes in fasting blood glucose between SB and SR.
Changes in total cholesterol (TC) in SRBaseline (pre-intervention) and 4 weeks (post-intervention)Changes in TC as measured via finger stick in SR.
Changes in triglyceride (TG) in SRBaseline (pre-intervention) and 4 weeks (post-intervention)Changes in TG as measured via finger stick in SR.
Changes in fasting blood glucose in SRBaseline (pre-intervention) and 4 weeks (post-intervention)Changes in fasting blood glucose as measured via finger stick in SR.
Changes in body fat in SRBaseline (pre-intervention) and 4 weeks (post-intervention)Changes in body fat as measured via BODPOD in SR.
Changes in weight in SRBaseline (pre-intervention) and 4 weeks (post-intervention)Changes in weight as measured via BODPOD in SR.
Changes in blood pressure in SRBaseline (pre-intervention) and 4 weeks (post-intervention)Changes in blood pressure as measured via Omron Digital BP Monitor HEM-907XL in SR.
Compared the changes in weight between SB and SRBaseline (pre-intervention) and 4 weeks (post-intervention)Compared the changes in weight between SB and SR.
Compared the changes in blood pressure between SB and SRBaseline (pre-intervention) and 4 weeks (post-intervention)Compared the changes in blood pressure between SB and SR.
Change in resting energy expenditure in SBBaseline (pre-intervention) and 4 weeks (post-intervention)Change in resting energy expenditure as measured by metabolic cart in SB.
Change in resting energy expenditure in SRBaseline (pre-intervention) and 4 weeks (post-intervention)Change in resting energy expenditure as measured by metabolic cart in SR.
Changes in high density lipoprotein (HDL) in SRBaseline (pre-intervention) and 4 weeks (post-intervention)Changes in HDL as measured via finger stick in SR.
Compared the changes in body fat between SB and SRBaseline (pre-intervention) and 4 weeks (post-intervention)Compared the changes in body fat between SB and SR.
Compared the changes in LDL between SB and SRBaseline (pre-intervention) and 4 weeks (post-intervention)Compared the changes in LDL between SB and SR.
Compared the changes in HDL between SB and SRBaseline (pre-intervention) and 4 weeks (post-intervention)Compared the changes in HDL between SB and SR.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026