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NCT ID: NCT04053686 Completed - Metabolic Syndrome Clinical Trials

An Intervention to Reduce Prolonged Sitting in Police Staff

Start date: September 9, 2019
Phase: N/A
Study type: Interventional

The primary aim of this study is to assess the feasibility of an intervention to reduce and break up prolonged sitting time in full-time police staff. The secondary aims of this study are to assess preliminary effects on patterns of sedentary behaviour (number of breaks, number of prolonged sitting bouts, average duration of prolonged sitting bouts, and total prolonged sitting duration), additional measures of sedentary behaviour (total sitting time, standing, and stepping), cardiometabolic risk markers, physiological stress (cortisol levels), physical health (self-report and postural stability), psychological wellbeing and mood, work stress (self-reported), and work performance (job satisfaction and productivity).

NCT ID: NCT04013451 Completed - Anxiety Clinical Trials

The Kiss of Kindness Study II

Start date: September 27, 2019
Phase: N/A
Study type: Interventional

The objective of this study is to assess the impact of engaging in deliberate acts of kindness on resilience (primary outcome); social interaction anxiety and affect (secondary outcomes); and mood (exploratory outcome) of undergraduate and graduate students at Western University (UWO). Recruitment of 200 participants consisting of 150 full-time undergraduate and 50 graduate students, randomized to either the intervention (n=100) or control group (n=100) will be achieved via a mass email to all full-time students at UWO. Both intervention and control groups will receive an email with access to a relaxation and stress management booklet from UWO's Wellness Education Centre (http://studentexperience.uwo.ca/docs/RelaxationAndStressManagement.pdf). In addition, the intervention group will be asked to (1) complete and log/submit a minimum of three deliberate acts of kindness per day for one month, and (2) join the study-dedicated online site to connect with, support, and share experiences and ideas with each other around acts of kindness. Individuals in the intervention group will also receive a list of deliberate acts of kindness ideas, for reference. Baseline, immediate post intervention, and three-months post intervention data will be collected using previously validated questionnaires associated with each outcome of interest, and posted to Qualtrics, an online survey tool. Additionally, immediately following the intervention and 3 months post intervention all participants will complete an open-ended question asking them to describe their overall experience being involved in the study. Quantitative and qualitative data analysis will occur upon the completion of the study.

NCT ID: NCT03953391 Completed - Affect Clinical Trials

The Effect of Tea Breaks on Cerebrovascular Perfusion During Desk Work

Start date: April 30, 2019
Phase: N/A
Study type: Interventional

Sedentary behaviour of healthy subjects may have a detrimental impact on cerebral blood flow as well as cognitive measures related to mood and alertness. In this study we focus on the impact of leaving the desk to consume a cup of tea at regular intervals during a sedentary working day.

NCT ID: NCT03839407 Completed - Anxiety Clinical Trials

The Impact of the MUSE Meditation Device on Student Registered Nurse Anesthetists

MUSE
Start date: February 20, 2019
Phase: N/A
Study type: Interventional

The question this study is designed to answer is whether or not the use of a MUSE Meditation Device lowers student registered nurse anesthetist's perception of stress, anxiety, and burnout within the Mayo Clinic Doctorate of Nurse Anesthesia Practice Program.

NCT ID: NCT03829813 Completed - Pain Clinical Trials

Effects of Music Therapy on Mood, Pain, Patient and Staff Satisfaction on Adult Inpatient Neurological Units

Start date: January 1, 2019
Phase: N/A
Study type: Interventional

A study examining the benefits of music therapy on patients, families, and unit staff on acute neurologic or inpatient rehabilitation units.

NCT ID: NCT03475836 Completed - Cognitive Change Clinical Trials

Cognitive Effects of Mint Essential Oil

Start date: March 14, 2016
Phase: N/A
Study type: Interventional

This study investigates the cognitive and mood effects of mint essential oils in a group of healthy, human adults. The investigational product will also be tested in vitro to ensure a number of biological mechanisms.

NCT ID: NCT03475823 Completed - Blood Pressure Clinical Trials

Cognitive and Blood Flow Effects of Mountain Tea

Start date: February 17, 2017
Phase: N/A
Study type: Interventional

Two doses (475 mg and 950 mg) of Sideritis Scardica (SS or 'mountain tea') are investigated for cognitive, mood, blood pressure and cerebral blood flow effects in a healthy group of 50-70 yr olds, both acutely and following 28 days of consumption.

NCT ID: NCT03404349 Completed - Stress Clinical Trials

Tailored Mindfulness Intervention in Adolescence

Start date: February 1, 2018
Phase: N/A
Study type: Interventional

Approximately 13%-20% of children living in the United States experience a mental health problem in any given year. Youth with mental illness have difficulty in social settings and have poor academic performance that place them at risk for increased stress and poor mental health outcomes. Stress typically manifests as depression, anxiety, or behavioral issues that lead to increasingly complex treatment with psychotropic medication. It would follow that reducing stress may be a way to improve psychological well being, prevent poor mental health outcomes, and hopefully avoid the need for psychotropic medication. Mindfulness teaching is a potentially powerful tool for adolescents because it focuses on reducing stress. Thus far, studies have not engaged adolescents in developing a patient-centered approach to mindfulness Interventions. The current project would be a significant contribution to clinical practice and the scientific evidence for mindfulness interventions. This research targets psychological well-being within a vulnerable adolescent population that is generally underrepresented in research. The research outcomes will be useful to healthcare providers, educators, and parents/families in encouraging optimal outcomes for adolescents. The overall goals of this proposed research project are to develop and assess the feasibility of an adolescent-developed mindfulness intervention.

NCT ID: NCT03221985 Completed - Communication Clinical Trials

ESM Pilot: Mobile Phones and Psychology

Start date: September 2016
Phase: N/A
Study type: Interventional

The research team will investigate whether there is a relation between smartphone usage and psychological parameters using the smartphone application.

NCT ID: NCT03190135 Completed - Physical Activity Clinical Trials

Evaluation of the BOKS Before-school Physical Activity Program

Start date: September 1, 2015
Phase: N/A
Study type: Interventional

BOKS, Build Our Kids' Success, is a before-school physical activity program that has been implemented in over 2,000 elementary and middle schools. Students participate in the program for 12 weeks, two or three mornings per week for about 1 hour per session. This study if a non-randomized control trial seeking to 1) examine the extent to which participation in the before-school BOKS program improves, health, well-being, and performance, and 2) compare the results of a two-day-per-week versus a three-day-per-week program.