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Psychological Distress clinical trials

View clinical trials related to Psychological Distress.

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NCT ID: NCT05229406 Completed - Depression Clinical Trials

Healthy Minds Program App Dosage

Start date: February 21, 2022
Phase: Phase 1
Study type: Interventional

The study will evaluate the effectiveness of the Healthy Minds Program (HMP) meditation app on participants experiencing depression and/or anxiety. Participants will be assigned to use the HMP app 5- or 15-minutes per day for 4 weeks.

NCT ID: NCT05228392 Completed - Clinical trials for Psychological Distress

The Effects of Listening to Lullabies and Self-selected Music on Distress and Maternal Attachment in Pregnant Women

Start date: June 16, 2021
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the effects of listening to lullabies and self-selected music at home in reducing the distress experienced in the prenatal period and increasing maternal attachment in pregnant women. This parallel randomized-controlled study was carried out at obstetrics outpatient clinics in Turkey. For two weeks and 30 minutes every day at home, the lullaby group (LG) only listened to the lullaby record selected by the researcher, while the multi-music group (MG) listened to self-selected music from different records presented to them by the researcher. The control group (CG) only received routine care. Prenatal distress and maternal attachment levels were assessed at the beginning and end of the intervention.

NCT ID: NCT05196464 Completed - Clinical trials for Psychological Distress

ACT Workshops: A Novel Delivery Modality to Increase Access to Care for Rural Veterans

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

This study investigates access, effectiveness, and acceptability of 1-day ACT workshops on problematic mental health symptoms.

NCT ID: NCT05130944 Completed - Stress Clinical Trials

Feasibility of Community Psychosocial Intervention for Women

Start date: September 9, 2021
Phase: N/A
Study type: Interventional

The purpose of the current protocol is to describe a cluster randomized feasibility trial examining the integration of a scalable stress management intervention into Entre Nosotras ('among/between us'), a community-based psychosocial intervention for migrant and host community women in Ecuador and Panamá. Specifically the study aims to: 1. Explore the relevance, acceptability, and feasibility of integrating a stress management intervention into community-based participatory women's group 2. Examine the feasibility of conducting a fully-powered cluster randomized controlled trial evaluating the effectiveness and implementation of integrating a stress management intervention into a community-based participatory women's group as compared to community-based participatory women's groups alone.

NCT ID: NCT05120453 Completed - Clinical trials for Psychological Distress

Interplay of Self-Criticism and Symptom Severity Over the Course of In-patient Psychotherapeutic Treatment

InSeCur
Start date: January 1, 2015
Phase:
Study type: Observational [Patient Registry]

The purpose of this study is to assess the interplay between self-criticism and symptom severity in patients undergoing psychotherapeutic treatment.

NCT ID: NCT05105646 Completed - Clinical trials for Psychological Distress

Are Perception of Pain and Psychological Distress Before Knee Arthroplasty Associated With Reason for Revision?

Start date: January 1, 2014
Phase:
Study type: Observational

The aim of our study is to identify the influence of preoperative pain (NRS pain score and EQ5D pain score) and higher levels of anxiety and depression (EQ5D anxiety/depression score) and their interaction before primary total knee arthroplasty on revision surgery for unexplained symptoms after primary surgery.

NCT ID: NCT05103488 Completed - Quality of Life Clinical Trials

Comprehensive Palliative Care for Cancer Patients in Vietnam

Start date: May 7, 2020
Phase: N/A
Study type: Interventional

There are exponential increases in cancer incidence and mortality worldwide and in Vietnam. Cancer affects patient's quality of life, which can be improved by palliative care. In Vietnam, due to a shortage in human resources for social workers, palliative care is mainly focused on medical aspect. A new comprehensive palliative care model, that provides multidisciplinary support including psychosocial support to patients, was developed. This research's objective is to evaluate the effectiveness of comprehensive palliative care (CPC) on improving the quality of life among cancer patients at a hospital in Vietnam. This randomized control trial is performed among 100 advanced cancer patients at University Medical Center at Ho Chi Minh city, Vietnam.The measurement tools include the Vietnamese Palliative Care Outcome Scale (VietPOS), the 5-level EQ-5D (EQ-5D-5L), Hospital Anxiety and Depression Scale (HADS) and Zarit Burden Interview (ZBI). Data collection has been conducting through face-to-face interviews three times: baseline, week 3, and week 6. Paired t-test (or Wilcoxon Rank sum test) and Student-t-test (or Mann -Whitney U test) will be used to evaluate and compare changes in quality of life and psychological distress within and between groups. Intention- to - treat analysis is used in the study. This is the first research that study the effectiveness of a palliative care psychosocial intervention on cancer patients in Vietnam. The result can be used to advocate for multidisciplinary palliative care in Vietnam.

NCT ID: NCT05092529 Completed - Depression Clinical Trials

Psychological Impact of COVID-19 on Intensive Care Survivors

PIM-COVID
Start date: November 17, 2020
Phase:
Study type: Observational

Psychological distress is commonly experienced by survivors of an intensive care admission, including patients treated during previous pandemics. Whilst data emerges about the short-term impact of COVID-19 on patients and healthcare systems, the long term impact remains unclear. The purpose of this trainee-led, multi-centre longitudinal study is to assess the short- and long-term psychological impact on patients who have survived an admission to intensive care due to COVID-19, and identify possible predictors of anxiety, depression and trauma symptoms in this patient group.

NCT ID: NCT05031611 Completed - Clinical trials for Psychological Distress

Intuitive Eating for Disordered Eating

IERCT
Start date: April 8, 2020
Phase: N/A
Study type: Interventional

Purpose: Research on intuitive eating is growing, but there are few interventions demonstrating the effect of learning to eat intuitively for people with disordered eating. Young women in particular are at high-risk for developing disordered eating. This study aimed to test the outcomes of a novel intuitive eating intervention for young women with disordered eating. Methods: This study is the first randomized controlled trial introducing intuitive eating to a sample of participants with disordered eating. Participants with current eating disorders were excluded from this study. Women (n=123) ages 18-30 with high levels of disordered eating participated in this study and were randomized to either a treatment (10-week web-based intervention) or control group (10-week waitlist).

NCT ID: NCT05013398 Completed - Clinical trials for Psychological Distress

The Together Webinar Programme For Military Partners

TTP-Webinar
Start date: May 7, 2019
Phase: N/A
Study type: Interventional

Military partners are at risk of mental health difficulties, including depression, anxiety and secondary traumatization. However, many partners face a range of barriers in accessing psychological support. As such, there remains a need to investigate how to make support for military partners more accessible. The present study was a pilot randomized controlled trial (RCT) investigating the effectiveness of The Together Webinar Programme (TTP-Webinar) in reducing psychological distress and secondary trauma symptoms and improving quality of life among partners of veterans with PTSD and other mental health difficulties. The pilot RCT compared the TTP-Webinar intervention to a waitlist condition. The primary aim was to assess the acceptability and feasibility of offering web-based support to military partners and to investigate the efficacy of the remote-access support. It was hypothesized that, compared to the waitlist condition, the TTP-Webinar would result in significant reductions in psychological distress and secondary symptoms, and improvements in overall quality of life.