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Stress, Psychological clinical trials

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NCT ID: NCT05734638 Recruiting - Hypertension Clinical Trials

Stress and Blood Pressure Management for Caregivers

Stress/HTN
Start date: September 11, 2023
Phase: N/A
Study type: Interventional

Due to health and wealth disparities, no demographic group is more at risk than African American women for the double jeopardy of stress from caregiving for persons living with dementia (PLWD) and stress associated with hypertension (HTN). This double jeopardy puts those they care for in jeopardy as well: Reduced quality of life and longevity, disability, cognitive decline, and stroke associated with HTN1 impede caregiving activities and resultant health and well-being for persons living with Alzheimer's disease and related dementias (ADRD). Although successful multi-component interventions have addressed ADRD caregiver stress (REACH II) and the Savvy Caregiver program, to our knowledge there are no interventions that target the complexity of chronic caregiving stress and HTN self-care for African American women caregivers of persons living with ADRD. This project will test two interventions for their effectiveness in improving outcomes for the target group: Mindfulness in Motion (MIM) and the Dietary Approaches to Stop Hypertension (DASH). MIM includes mindful awareness and movement from a seated position, breathing exercises, healthy sleep, and guided mindfulness meditation. The DASH component will be tailored for Black Americans. It uses a critical thinking approach that involves problem solving, participant-centered goal setting, health coaching, reflection, and development of self-efficacy (confidence) to promote physical activity and healthy eating. Solid empirical evidence demonstrates its effectiveness in reducing blood pressure among mixed-race samples.

NCT ID: NCT05724420 Recruiting - Stress, Emotional Clinical Trials

STRIVE - Resilience Curriculum for Novice Physicians-In-Training

Start date: April 4, 2023
Phase: N/A
Study type: Interventional

The goal of this trial is to compare self-reported resilience scores in junior physicians-in-training after completion of formal resilience training. The main questions this trial aims to answer are: - Does formal resilience training improve self-reported resilience scores? - Does the timing of resilience training (i.e., first vs second year of residency training) impact the effect of training? All participants will be provided with resources on resilience and learner support as per usual institutional practice. The intervention group will also participate in a formal resilience training program. Researchers will compare self-reported resilience scores 3 months after training to determine the effect of the training program.

NCT ID: NCT05721482 Active, not recruiting - Hypertension Clinical Trials

Stress and Hypertension in Dementia Caregivers

MIM-DASH
Start date: January 17, 2023
Phase: N/A
Study type: Interventional

No demographic group is more at risk for the double jeopardy of caregiving stress and hypertension (HTN) than African American women caring for a family member with Alzheimer's disease and related dementias (ADRD). Both situations lead to reduced quality of life and cardiovascular disease-a complication of uncontrolled hypertension. Maintaining the health of these caregivers is critical to support the well-being of the care recipients. Although some multi-component interventions have addressed ADRD caregiver's stress and quality of life, gaps remain in targeting interventions to address the complexity of chronic caregiving stress and hypertension self-care in African American women. This pilot study builds on the investigator's earlier work which showed that stress, blood pressure knowledge, and complex diet information deficits all interfered with older African American women's hypertension self-care. Lifestyle changes (stress management, reducing sodium, eating fruits/vegetables, and physical activity) are effective in managing hypertension. The investigator's Stage I pilot study is based on the scientific rationale that these lifestyle changes can be promoted by addressing stress reactivity/stress resilience, the psychological and physiological response of the body to stress, as the underlying mechanism to facilitate behavioral change. In this way the study can improve health outcomes (caregiver stress, quality of life, cardiovascular disease risk).

NCT ID: NCT05703165 Not yet recruiting - Clinical trials for Psychological Stress

Horse-assisted Intervention, Heart Rate Variability & Stress

Start date: March 1, 2023
Phase: N/A
Study type: Interventional

In this study, the effects of an animal-assisted intervention on people with increased stress levels are investigated. The data collected will be compared with those of participants with high stress levels but without animal-assisted intervention (participants only observe nature) and with a control group consisting of people without stress exposure. The study will be performed in the following setting: Questionnaire examination on chronic stress, questionnaire on current well-being and heart rate variability (HRV) measurement before the horse-assisted intervention, one HRV measurement and one questionnaire examination (POMS) on current well-being after the horse-assisted intervention, one questionnaire (POMS) on current well-being 5 days after the horse-assisted intervention.

NCT ID: NCT05703087 Completed - Clinical trials for Osteoarthritis, Knee

Positive Cueing in Knee Arthroplasty.

Start date: September 21, 2021
Phase: N/A
Study type: Interventional

To the knowledge of the investigators, the feasibility of an RCT assessing the use of positive cueing in an information video for patients undergoing primary TKA is currently unclear. The investigators conducted a feasibility study with the primary objective to assess the acceptability of the randomized controlled trial (RCT) procedure for participating patients. The secondary objective was to evaluate the rate of recruitment, the comprehensibility (do patients understand what is expected of them during the trial) and if there were any adjustments necessary to the design of the study. The outcome of the current feasibility study will be used to determine whether adjustments are required to the design of the RCT before we proceed.

NCT ID: NCT05688254 Completed - Clinical trials for Stress, Psychological

Internet-Based Stress Recovery Program for Adolescents

FOREST-A
Start date: April 25, 2023
Phase: N/A
Study type: Interventional

The study aims to evaluate the feasibility and efficacy of the internet-based stress recovery program for adolescents.

NCT ID: NCT05681013 Completed - Insomnia Clinical Trials

The Effect of Laughter Therapy on Nursing Students

Therapy
Start date: February 1, 2021
Phase: N/A
Study type: Interventional

The aim of this study is to determine the effect of laughter therapy on the general health status, sleep quality, and stress level of nursing students.

NCT ID: NCT05640505 Completed - Clinical trials for Stress, Psychological

Gratitude Interventions for Academic Stress Among Pakistani Adolescents

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

The experimental nature of this study will provide the empirical data in analyzing the effectiveness of gratitude exercises which later can be adapted in stress reduction programs at school level. This research will focus on the school related positive life experiences for example thinking about a teacher/mentor kindness and contribution in their lives, then write a letter that describes their gratitude & letter will be delivered to that person indirectly. This may help in focusing on the positive aspects of school life. This modification will serve as testing this new model for assessing the combined effect of gratitude interventions.

NCT ID: NCT05638152 Not yet recruiting - Pain, Postoperative Clinical Trials

Effect of a Bundle of Non-pharmacological Interventions on the Stress Response to Surgery

SPACU-lab
Start date: May 1, 2023
Phase:
Study type: Observational

Rationale: Surgical trauma and post-surgical pain induce a physiological stress response that can be detrimental to the patient. Non-pharmacological interventions aimed at stress reduction are known to reduce pain scores and opioid consumption. The effect of these interventions on the surgical stress response are unknown. Objective: To assess the effect of a bundle of non-pharmacological interventions implemented in the post-anesthesia care unit on the total serum cortisol levels after intermediate and major surgery. Study design: This is a prospective before-after study. Study population: Patients scheduled for intermediate or major oncological surgery in a tertiary referral cancer center. Intervention: The implementation of a bundle of four non-pharmacological interventions aimed at stress reduction in the post-anesthesia care unit. The bundle consists of: access to music, aromatherapy, natural images on the walls and ceiling and communication techniques aimed at reduction of stress and pain. Main study parameters/endpoints: Serum cortisol levels on the first postoperative day.

NCT ID: NCT05637736 Active, not recruiting - Nurse's Role Clinical Trials

Effects of an Immersive Virtual Reality Intervention

Start date: March 1, 2022
Phase: N/A
Study type: Interventional

Some recent studies demonstrated caregivers may experience negative emotions such as anxiety and sadness, which may also affect normal treatment during the epidemic. As the pandemic continues, mental health support, encouragement , and a sense of purpose are needed to support healthcare workers.