Clinical trials: Stress, completed
Diabetes Mellitus, Stress, Psychological
A Mind-Body Intervention for Diabetes Management: A Pilot Study
Managing type 1 diabetes is stressful. Stress physiology influences glucose metabolism. Continuous glucose monitors allow us to track glucose variability in the real-world environment.
- Conditions
- Diabetes Mellitus, Stress, Psychological, Stress, Physiological
- Trial name
- NCT04944264
- Testing
- Stress Management and Resiliency Training (SMART) program
- Where
- United States
- Volunteers
- 34 people, healthy volunteers welcome
- Sponsor
- Dartmouth-Hitchcock Medical Center
Post-traumatic Stress Disorder, Post-Traumatic Stress Disorder, Chronic
PTSD Affect Labeling Study
The overall goal of this study is to use fMRI and psychophysiological measures to investigate a novel strategy involving "Affect Labeling" for improving emotion regulation in PTSD that could lead to a new treatment regimen for…
- Trial name
- NCT05924399
- Testing
- Affect Labeling Training
- Where
- United States
- Volunteers
- 119 people, healthy volunteers welcome
- Sponsor
- University of California, Los Angeles
Stress Reaction, Nurse's Role
Mindfulness Meditation for Nursing Students
Mindfulness meditation was used to reduce stress and its responses such as cortisol and C-reactive protein (CRP) among healthy and ill individuals in various cultures, but their effects have not yet been studied among Jordanian…
- Trial name
- NCT05099224
- Testing
- Mindfulness meditation
- Where
- Jordan
- Volunteers
- 108 people, healthy volunteers welcome
- Sponsor
- Jordan University of Science and Technology
Restlessness, Pain
Effects of Dexmedetomidine on Stress Response and Postoperative Analgesia
Dexmedetomidine is a highly selective α2 adrenoreceptor agonist approved by the US FDA for short-term postoperative sedation and analgesia.It can also reduce the stress response without respiratory depression.
- Trial name
- NCT01517932
- Testing
- dexmedetomidine
- Volunteers
- 60 people
- Sponsor
- Fang Luo
Type 2 Diabetes Mellitus
Effects of Dietary Supplement Tauroursodeoxycholic Acid on Vascular Function
The purpose of the present study is to determine if use of dietary supplement tauroursodeoxycholic acid enhances insulin-stimulated leg blood flow and glucose disposal.
- Trial name
- NCT03331432
- Testing
- Tauroursodeoxycholic acid
- Where
- United States
- Volunteers
- 8 people
- Sponsor
- University of Missouri-Columbia
Burnout, Professional, Self Compassion
Better Together Physician Coaching to Mitigate Burnout Amongst Clinicians
Better Together Physician Coaching ("Better Together", or "BT"), a 4-month, web-based positive psychology multimodal coaching program was built to decrease burnout in medical trainees.
- Conditions
- Burnout, Professional, Self Compassion, Flourishing, Imposter Syndrome
- Trial name
- NCT05635448
- Testing
- Better Together Physician Coaching Program, No intervention - waitlist control
- Where
- United States
- Volunteers
- 160 people, healthy volunteers welcome
- Sponsor
- University of Colorado, Denver
Chronic Pain, Back Pain
Group-based Mindfulness for Chronic Pain in the Primary Care Setting
The purpose of this pragmatic clinical trial (PCT) research is to determine whether a group-visit approach modeled on Mindfulness-Based Stress Reduction can improve function for persons with chronic low back pain.
- Trial name
- OPTIMUM (NCT04129450)
- Testing
- Group medical visits with mindfulness-based stress reduction, Usual PCP care
- Where
- United States
- Volunteers
- 451 people
- Sponsor
- Boston Medical Center
Posttraumatic Stress Disorder, Traumatic Brain Injury
3MDR to Treat PTSD With mTBI (3MDR)
Background and Purpose: Posttraumatic stress disorder (PTSD) and mild traumatic brain injury (mTBI) are persistent and frequently comorbid complications of recent combat.
- Trial name
- 3MDR (NCT03796936)
- Testing
- Motion-assisted, Multi-modular Memory Desensitization and Reconsolidation (3MDR) Therapy
- Where
- United States
- Volunteers
- 20 people
- Sponsor
- Walter Reed National Military Medical Center
Urinary Incontinence, Stress
Duloxetine Stress Urinary Incontinence Efficacy and Safety Study
Study F1J-MC-SBBU will examine the effect of duloxetine treatment in women with SUI. The inclusion and exclusion criteria of this Phase 3 study will ensure that all subjects have a clinical diagnosis of SUI.
- Trial name
- NCT00475397
- Testing
- Duloxetine
- Where
- South Korea
- Volunteers
- 120 people, healthy volunteers welcome
- Sponsor
- Eli Lilly and Company
Laughter Yoga
The Effect of Laughter Yoga on the Anxiety and Stress Levels of Women in the Postpartum Period
This research is a randomized controlled study to evaluate the effect of Laughter yoga on the anxiety and stress levels of postpartum women.
- Trial name
- NCT05345067
- Testing
- Experimental: Laughter yoga session parts-1, Experimental: Laughter yoga session parts-2, Experimental: Laughter yoga session parts-3
- Where
- Turkey (Türkiye)
- Volunteers
- 144 people, healthy volunteers welcome
- Sponsor
- Ataturk University
Endoplasmic Reticulum Stress, Viral Infection
Modulate Cellular Stress in the Immune Cells to Reduce Rate of Symptomatic Viral Infection
To determine the efficacy of metformin in reducing the rate of symptomatic YF17D infection, and to elucidate the effects of metformin on YF17D viremia and the downstream adaptive immune response, we hereby propose a randomised…
- Conditions
- Endoplasmic Reticulum Stress, Viral Infection, Yellow Fever
- Trial name
- NCT04267809
- Testing
- Metformin Hydrochloride, Calcium and Vitamin D
- Where
- Singapore
- Volunteers
- 32 people, healthy volunteers welcome
- Sponsor
- Singapore General Hospital
Periodontal Health, Periodontitis Stage III
EVALUATION OF SALIVA AND SERUM HEME OXYGENASE, ARYLESTERASE AND NUCLEAR FACTOR ERYTHROID 2-RELATED FACTOR 2 LEVELS IN PATIENTS WITH STAGE III PERIODONTITIS
Periodontal disease is a chronic and progressive inflammatory disease in which the hard and soft tissues that support the teeth are damaged.
- Trial name
- NCT06986044
- Testing
- Serum Total Oxidant Status, Salivary Total Oxidant Status, Serum Total Antioxidant Status
- Where
- Turkey (Türkiye)
- Volunteers
- 74 people, healthy volunteers welcome
- Sponsor
- Saglik Bilimleri Universitesi
Urinary Incontinence, Stress Urinary Incontinence
Efficacy of the Use of Vaginal Balls for the Improvement of Urinary Incontinence and Sexual Function in Women.
Asess if adding vaginal spheres treatment to the conventional Pelvic Floor Muscle Trainning (PFMT) produces a greater decrease in the severity of the stress urinary incontinence or a greater perceived quality of life related to…
- Conditions
- Urinary Incontinence, Stress Urinary Incontinence, Sexual Dysfunction
- Trial name
- NCT05732844
- Testing
- Intervention group with Enna pelvic ball, Control group
- Where
- Spain
- Volunteers
- 64 people
- Sponsor
- RAPbarcelona
Exhaustion; Syndrome
Assessing the Impact of Acupuncture Therapy on Medical Resident Well-Being: Feasibility and Acceptance
This feasibility study develops methods for larger-scale research, evaluating the acceptability and perceived impact of a group acupuncture and acupressure intervention, as well as suitability of a self-report instrument.
- Trial name
- NCT03245034
- Testing
- Auricular Acupuncture Therapy
- Where
- United States
- Volunteers
- 12 people, healthy volunteers welcome
- Sponsor
- NYU Langone Health
Urodynamic Stress Incontinence
Comparison Between Positive and Negative sUPP
Urodynamic stress incontinence is a prevalent condition among women, characterized by involuntary urine leakage during activities that increase intra-abdominal pressure, such as coughing, sneezing, or physical exertion.
- Trial name
- NCT06783699
- Where
- Taiwan
- Volunteers
- 481 people
- Sponsor
- National Taiwan University Hospital
Stress Urinary Incontinence
To Evaluate the Safety in Patients Taking Duloxetine for Stress Urinary Incontinence
This is an on-going study to evaluate the long-term safety and maintenance of effect of duloxetine in patients suffering with stress urinary incontinence.
- Trial name
- NCT00190632
- Testing
- Duloxetine
- Where
- United States
- Volunteers
- 600 people
- Sponsor
- Eli Lilly and Company
Trauma Injury, Child, Only
Using mHealth to Improve Emotional Recovery After Pediatric Injury
Nearly 300,000 U.S. children experience injuries that require them to be hospitalized this year. These children, and their caregivers, are at high risk for emotional and behavioral problems, as well as poor quality of life.
- Conditions
- Trauma Injury, Child, Only, Posttraumatic Stress Disorder, Parents
- Trial name
- NCT04579198
- Testing
- Caregivers' Aid to Accelerate Recovery after pediatric Emergencies (CAARE)
- Where
- United States
- Volunteers
- 54 people, healthy volunteers welcome
- Sponsor
- Medical University of South Carolina
Perceived Stress, Persistent Poverty
Pathways to Empowerment for Persons Living in Persistent Poverty
The general purpose of this feasibility study is to evaluate the potential impact of Pathways to Empowerment (PTE) on the four constitutional conditions of social quality for persons living in persistent poverty.
- Trial name
- NCT05336097
- Testing
- Pathways to Empowerment
- Where
- Netherlands
- Volunteers
- 35 people, healthy volunteers welcome
- Sponsor
- Radboud University Medical Center
Posttraumatic Stress Disorder (PTSD)
Acupuncture for the Treatment of Posttraumatic Stress Among Military Personnel
The purpose of this study is to determine the effectiveness of acupuncture as a treatment for Posttraumatic Stress Disorder (PTSD) among military personnel.
- Trial name
- NCT00320138
- Testing
- Acupuncture, using Chinese Medicine methodology
- Where
- United States
- Volunteers
- 55 people
- Sponsor
- Henry M. Jackson Foundation for the Advancement of Military Medicine
Breast Cancer
Green Tea and Reduction of Breast Cancer Risk
RATIONALE: Green tea extract contains ingredients (catechins) that may lower the risk of breast cancer. PURPOSE: This phase II trial is studying how well green tea extract works in preventing breast cancer compared to a placebo…
- Trial name
- NCT00917735
- Testing
- Green tea extract supplement
- Where
- 5 sites in United States
- Volunteers
- 1,075 people, healthy volunteers welcome
- Sponsor
- University of Minnesota
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