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Coping Skills clinical trials

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NCT ID: NCT04720014 Active, not recruiting - Clinical trials for Stress, Psychological

Enhancing Resilience in Senior Living Community Residents

Start date: March 30, 2021
Phase: N/A
Study type: Interventional

This single-arm pilot study tests the feasibility of integrating the Stress Management and Resiliency Training Relaxation Response Resiliency Program (SMART-3RP), a mind-body intervention, into senior living residential communities. The investigators hypothesize that the SMART-3RP intervention will be feasible for senior living community residents to attend.

NCT ID: NCT04646642 Completed - Covid19 Clinical Trials

Psychological Health, Coping Strategies and Preferences of Military COVID-19 Deployers

Start date: December 14, 2020
Phase:
Study type: Observational

The proposed research study aims to better understand COVID deployer needs. The study, informally referred to as Project COPE, asks David Grant U.S. Air Force Medical Center (DGMC) members who deployed in support of COVID-19 operations to complete a needs assessment questionnaire. The purpose of this study is to understand the stressful experiences of our COVID Theater Hospital (CTH) deployers, the typical coping strategies used and recommended preferences for support so that the investigators can provide the best evidence-based resources for post-deployment and to aid future CTH deployers.

NCT ID: NCT04629300 Active, not recruiting - Quality of Life Clinical Trials

Supportive Care Mobile Application for Patients With NSCLC

Start date: October 15, 2021
Phase: N/A
Study type: Interventional

This research study is looking at the role of a supportive care mobile app in improving symptoms, coping skills, and quality of life in patients with non-small cell lung cancer.

NCT ID: NCT04525183 Active, not recruiting - Ovarian Cancer Clinical Trials

REVITALIZE: A Telehealth Intervention for Women With Advanced Ovarian Cancer and PARP Inhibitor-Related Fatigue

Start date: December 2, 2020
Phase: N/A
Study type: Interventional

This study is testing whether a 6 week skills-based telehealth intervention can help ovarian cancer patients experiencing PARP inhibitor-related fatigue reduce the impact of fatigue on their daily life and activities.

NCT ID: NCT04479995 Active, not recruiting - Quality of Life Clinical Trials

Multidisciplinary Intervention In Chronic GVHD

Start date: August 2, 2020
Phase: N/A
Study type: Interventional

This research is being done to evaluate the feasibility and efficacy of a multidisciplinary, patient-centered intervention, Horizons Program, versus minimally enhanced standard care to improve quality of life, symptom burden and psychological distress of adults who received an allogeneic hematopoietic stem cell transplant and developed graft versus-host disease (GVHD).

NCT ID: NCT04474158 Recruiting - Adolescent Behavior Clinical Trials

Creating Peace: Community-based Youth Violence Prevention to Address Racism and Discrimination

Start date: December 4, 2020
Phase: N/A
Study type: Interventional

This cluster-randomized community-partnered study will examine the effectiveness of a trauma-sensitive, gender transformative youth violence prevention program called Creating Peace that integrates racism and discrimination prevention with youth ages 14-19.

NCT ID: NCT04426266 Completed - COVID-19 Pandemic Clinical Trials

Psychological Effects of the COVID-19 Pandemic on the Hungarian Adult Population

Start date: May 1, 2020
Phase:
Study type: Observational

The aim of the study is to explore the psychological effects of the COVID-19 pandemic among Hungarian adults with the use of an anonymous online questionnaire that consists of 65 items. With these results it will possible to identify coping strategies that can help Hungarian adults to deal with the difficulties arising from the pandemic.

NCT ID: NCT04388696 Completed - Adolescent Behavior Clinical Trials

A Feasibility Trial of Sisterhood 2.0

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

This pilot quasi-experimental community based trial examines the feasibility of a sexual violence and adolescent relationship abuse prevention program for girls aged 14-19. Feasibility is assessed through participant attendance, retention and program satisfaction measures and interviews are conducted at baseline, end of program and 3 month follow up (endline) about participant experiences.

NCT ID: NCT04386655 Completed - Clinical trials for Traumatic Brain Injury

Brain Injury Coping Skills - Telemedicine: Phase II

BICS-T-2
Start date: March 28, 2019
Phase: N/A
Study type: Interventional

For phase II, the objective is to compare the effectiveness of BICS-T with the well-established BICS in-person group. Information gained from phase I (the feasibility study) was used to make necessary changes to the BICS-T protocol. The purpose of this study is to provide survivors of brain injury and caregivers greater support and teach adaptive coping strategies, through a designed and studied a coping skills group specifically for brain injury survivors and their caregivers at the Rehabilitation Hospital of Indiana (RHI) called the Brain Injury Coping Skills group (BICS).

NCT ID: NCT04371211 Completed - Clinical trials for Traumatic Brain Injury

Telemedicine Brain Injury Coping Skills (BICS-T) Support Group for Brain Injury Survivors and Their Caregivers

BICS-T I
Start date: September 20, 2018
Phase: N/A
Study type: Interventional

Brain Injury can be devastating for both patients and family members and can result in chronic difficulties in vocational, social, financial, as well as physical functioning. The occurrence of emotional and neurobehavioral challenges in individuals with brain injury is also common with research consistently showing links between these challenges and a person's overall rehabilitation outcome. In order to provide patients and caregivers greater support and teach adaptive coping strategies, the authors of this grant designed and studied a coping skills group specifically for brain injury survivors and their caregivers at the Rehabilitation Hospital of Indiana (RHI) called the Brain Injury Coping Skills group (BICS). BICS is a 12 session (one session per week), manualized, cognitive-behavioral treatment group designed to provide support, coping skills, and psychoeducation aimed to improve perceived self-efficacy (PSE) and emotional functioning.