Emotional Distress

18

Review clinical trials related to Emotional Distress. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Mindfulness Intervention for Emotional Distress (MIED) in Patients With GERD

The goal of this multicenter randomized waitlist-controlled clinical trial is to evaluate whether an online Mindfulness-Based Intervention for Emotional Distress (MIED) can reduce emotional distress and reflux-related symptoms in adults with gastroesophageal reflux disease (GERD). GERD is a common chronic gastrointestinal condition that is frequently accompanied by anxiety, depressive symptoms, stress, and impaired quality of life. The main questions this study aims to answer are: Can online MIED reduce emotional distress in patients with GERD? Can online MIED reduce reflux-related symptoms and improve reflux-related quality of life? Are changes in psychological processes, such as distress tolerance, cognitive flexibility, experiential avoidance, emotional behaviors, and life engagement, associated with improvements in emotional distress and reflux symptoms? Researchers will compare participants receiving online MIED with participants in a waitlist control group receiving usual medical care and health management to determine whether online MIED leads to greater improvement over time. Participants will: complete screening and baseline assessments; be randomly assigned to either the online MIED intervention group or the waitlist control group; if assigned to the intervention group, complete an 8-week online MIED program with one session per week; continue necessary usual medical care during the study, while keeping medication use stable when possible; complete online questionnaires at baseline, during the intervention, after the intervention, and at 3, 6, 12, and 24 months after the intervention; report information on reflux symptoms, emotional distress, quality of life, sleep, stress, resilience, life satisfaction, healthcare use, intervention adherence, and adverse events.

Participants needed: 500
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Xinghua LiuUpdated: Jun 25, 2026Locations: 15
Eligibility criteria

Aged 18 to 65 years. [+5]

Alarm symptoms or high suspicion of serious organic disease, including but not l... [+6]

Status: Not yet recruiting

Emotional Distress and Pathologic Response in Locally Advanced Gastric/GEJ Adenocarcinoma

This is a single-center, prospective observational cohort study designed to evaluate the association between pretreatment emotional distress and pathologic response to perioperative immunotherapy in patients with locally advanced gastric or gastroesophageal junction adenocarcinoma. A total of 120 patients planned for neoadjuvant immunotherapy followed by curative surgery will be enrolled. Emotional distress will be assessed using the PHQ-9 and GAD-7 before treatment initiation and at prespecified time points during treatment. Participants will be classified into an emotional distress group or a non-emotional distress group according to predefined criteria. The primary endpoint is major pathological response (MPR). Secondary endpoints include pathological complete response (pCR), R0 resection rate, event-free survival (EFS), recurrence-free survival (RFS), and overall survival (OS). Exploratory analyses will assess dynamic changes in emotional distress and their associations with peripheral stress markers, peripheral immune markers, and tumor immune microenvironment features.

Participants needed: 120
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: West China Second University HospitalUpdated: Jun 23, 2026Duration: 3 Years
Eligibility criteria

Willing to participate in this study. [+8]

Presence of distant metastasis, peritoneal metastasis, or loss of curative treat... [+4]

Status: Recruiting

Auricular Acupuncture on Emotional Distress in Service Members and Veterans With PTSD

Emotional distress (ED) refers to a state of mental suffering that significantly impairs an individual's ability to cope, often leading to a decline in overall well-being. In military contexts, ED is a prevalent concern due to the unique and demanding challenges faced by military personnel both in combat zones and during peacetime. The primary objective of this study is to assess the efficacy of integrating ear acupuncture with mindfulness therapy in mitigating ED and alleviating post-traumatic stress disorder (PTSD) symptoms among military personnel. The study will examine the effects of auricular acupuncture (AA) and mindfulness therapy (MT) on ED in military personnel with PTSD. The NADA ear acupuncture protocol will be administered using acupuncture semi-permanent (ASP), sterile needles placed in the bilateral ears, which will remain in place until they naturally fall out. Mindfulness therapy will incorporate relaxation techniques, such as yoga and controlled breathing exercises, specifically designed to alleviate ED. A mixed-methods approach, integrating both quantitative and qualitative methods, will be employed concurrently to evaluate the interventions' effectiveness and to explore the participants' perceived benefits. Specific Aim 1: To evaluate the effectiveness and perceived benefits of the National Acupuncture Detoxification Association (NADA) ear acupuncture protocol as an adjunct therapy to brief mindfulness therapy for reducing emotional distress in service members and veterans with PTSD. Specific Aim 2: To examine the effectiveness of NADA as an adjunct therapy to brief mindfulness therapy in improving sleep disturbances, alcohol use, and pain in service members and veterans with PTSD.

Participants needed: 66
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: United States Naval Medical Center, San DiegoUpdated: Apr 24, 2026Locations: 2
Eligibility criteria

Active duty service member and veterans [+4]

Status: Recruiting

Emerging Technologies and Teen Mental Health

This study will recruit teens who are experiencing subacute suicidal ideation to test the effect of a brief psychoeducational intervention focused on social media use wherein youth learn about active and prosocial use of social media platforms.

Participants needed: 200
Trial details
Age: 12-17Biological sex: AllType: InterventionalSponsor: Florida International UniversityUpdated: Apr 14, 2026Locations: 1
Eligibility criteria

Adolescents must (A) be between ages 12 and 17 years [+4]

Adolescents must not (A) have cognitive impairment or developmental delay which... [+1]

Status: Not yet recruiting

A Novel Auditory Application for Distraction in Pediatric Patients

This mixed-methods study seeks to evaluate the feasibility of Mystic Pets software and hardware within the pediatric population. This study will take place at Lucile Packard Children's Hospital (Stanford University, Palo Alto, CA).

Participants needed: 20
Trial details
Age: 4-17Biological sex: AllType: InterventionalSponsor: Stanford UniversityUpdated: Mar 23, 2026Locations: 1
Eligibility criteria

Between 4-17 years [+1]

Legal guardian not present to obtain consent [+6]

Status: Recruiting

Neurostimulation Versus Therapy for Problems With Emotions

The primary goal of this clinical trial is to evaluate the unique neural and behavioral effects of a one-session training combining emotion regulation skills training, with excitatory repetitive transcranial magnetic stimulation (rTMS) over the dorsolateral prefrontal cortex (dlPFC). The secondary aim is to identify key changes in the emotion regulation neural network following the combined intervention versus each of the components alone. The third aim is to explore personalized biomarkers for response to emotion regulation training. Participants will undergo brain imaging while engaging in an emotional regulation task. Participants will be randomly assigned to learn one of two emotion regulation skills. Participants will be reminded of recent stressors and will undergo different types of neurostimulation, targeted using fMRI (functional MRI) results. Participants who may practice their emotion regulation skills during neurostimulation in a one-time session. Following this training, participants will undergo another fMRI and an exit interview to assess for immediate neural and behavioral changes. Measures of emotion regulation will be assessed at a one week and a one month follow up visit.

Participants needed: 240
Trial details
Age: 18-55Biological sex: AllType: InterventionalSponsor: Duke UniversityUpdated: Mar 4, 2026Locations: 1
Eligibility criteria

age 18 to 55 [+6]

current hypomania (Note: Bipolar II w/o current hypomanic episode is ok for incl... [+21]

Status: Recruiting

Impact of Emotional Status on Prognosis of Patients With BCLC Stage B/C Hepatocellular Carcinoma Undergoing Hepatic Arterial Infusion Chemotherapy Combined With Targeted and Immunotherapy

This study is a multicenter, prospective, observational clinical trial designed to evaluate the impact of baseline emotional status on the clinical outcomes of patients with BCLC stage B/C hepatocellular carcinoma undergoing HAIC combined with targeted immunotherapy. A total of 90 patients are planned to be enrolled and divided into a depressive mood group and a non-depressive mood group based on a PHQ-9/GAD-7 score of ≥5 points. The primary study endpoint is progression-free survival (PFS), and the secondary endpoints include objective response rate (ORR), disease control rate (DCR), overall survival (OS), and safety profile. Dynamic assessments of patients' emotional status, quality of life (EORTC QLQ-C30), and peripheral blood levels of neuroendocrine-immune markers will be conducted at preset time points. The results indicate that emotional status may serve as an important modifiable factor influencing the efficacy of comprehensive therapy in patients with advanced liver cancer, providing an evidence-based basis for the formulation of psychosomatic integrated clinical intervention strategies in the future.

Participants needed: 90
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Nanfang Hospital, Southern Medical UniversityUpdated: Feb 27, 2026Locations: 1Duration: 2 Years
Eligibility criteria

1: All patients provided voluntary, written informed consent prior to any study...

Status: Not yet recruiting

The Coma Family Program (COMA-F): A Resilience Program for Caregivers of Patients With Severe Acute Brain Injury

The purpose of this research study is to determine whether COMA-F is more efficacious at reducing emotional distress in caregivers of patients with severe acute brain injuries, compared to health education control.

Participants needed: 150
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Massachusetts General HospitalUpdated: Feb 20, 2026Locations: 3
Eligibility criteria

18 years or older - study population [+9]

1. Serious mental illness, substance misuse, or active suicidal intent or plan -...

Status: Recruiting

Intervention to Prevent Behavioral Health Symptoms Among Pandemic Affected Children

Racial and ethnic minority children who live in socioeconomically disadvantaged communities are disproportionately impacted by pandemic and climate-induced disasters. Although effective interventions have been designed to treat mental health related symptoms in post-disaster settings, accessible, empirically supported prevention interventions are needed to prevent the onset of mental and behavioral health issues among these children. Building on our preliminary findings, the proposed study examines the efficacy and implementation of a COVID-19 adapted disaster focused prevention intervention, Journey of Hope-C19, in preventing behavioral health and interpersonal problems among racial and ethnic minority children who live in low-resource high poverty communities.

Participants needed: 800
Trial details
Age: 8-14Biological sex: AllType: InterventionalSponsor: University of Illinois at Urbana-ChampaignUpdated: Jan 23, 2026Locations: 9
Eligibility criteria

child experienced the COVID-19 pandemic and an additional large-scale disaster [+4]

child is currently receiving treatment for a diagnosed mental health condition [+1]

Status: Not yet recruiting

Promoting Positive Emotions in Adolescents Using Positive Events Training: An Indicated Approach

Research shows that high positive emotionality is an essential ingredient in building resilience in youngsters, especially those with a vulnerability to develop depressive symptomatology. It may empower them against actual depression and its various long-term adverse outcomes. One way to achieve positive emotions is via the recollection and anticipation of specific positive events. Therefore, to cultivate positive emotions in young people, a user-friendly group training program was developed, translated from basic research findings: Positive Event Training (PET). Through PET, adolescents learn to solidify positive memories and positive plans for the future. In this project, a comprehensive evaluation of PET's efficacy is conducted using a robust methodology with vulnerable youth.

Participants needed: 36
Trial details
Age: 12-16Biological sex: AllType: InterventionalSponsor: KU LeuvenUpdated: Dec 17, 2025
Eligibility criteria

12-16 years (age) [+1]

Status: Not yet recruiting

Resiliency Intervention for Patients With ALS and Their Care-Partners

The purpose of this study is to pilot a resiliency and coping intervention for persons recently diagnosed with Amyotrophic Lateral Sclerosis (ALS) and their primary informal caregivers. The data investigators gather in this study will be used to further refine our intervention.

Participants needed: 20
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Massachusetts General HospitalUpdated: Nov 17, 2025Locations: 1
Eligibility criteria

recent (within ~2 months) of first appointment at Healey Center for diagnosis of... [+5]

patient with ALS with comorbid terminal diagnosis or severe mental health disord... [+2]

Status: Recruiting

Mind-body Resilience Program for Cardiac Arrest Survivors and Their Caregivers: Recovering Together After Cardiac Arrest

The purpose of this study is to pilot two resilience interventions for cardiac arrest survivors and their informal caregivers, Recovering Together after Cardiac Arrest 1 and Recovering Together after Cardiac Arrest 2 . The data the investigators gather in this study will be used to further refine the interventions.

Participants needed: 84
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Massachusetts General HospitalUpdated: Oct 23, 2025Locations: 1
Eligibility criteria

Out-of-hospital or in-hospital CA survivor (must have new diagnosis of "cardiac... [+4]

active psychosis, mania, substance dependence, or suicidal intent or plan that w... [+2]

Status: Not yet recruiting

Therapeutic Writing for Adults Suffering From Chronic Pain and Comorbid Mental Health Disorders

The goal of this observational study is to understand the effects and experiences of therapeutic writing interventions in adult women with chronic pain and co-occurring mental health conditions. The main questions it aims to answer are: Can therapeutic writing help relieve chronic pain and emotional distress? How does writing support emotional processing, regulation, and meaning-making during rehabilitation? Participants will take part in a two-part writing intervention involving: Guided writing exercises that focus on emotional processing, emotion regulation, and creating meaning. Individual interviews after the writing sessions to explore their experiences. The study uses qualitative analysis methods-phenomenology and logotherapy-to better understand how these writing interventions may support recovery, improve well-being, and offer non-pharmacological tools for managing chronic pain and mental health challenges.

Participants needed: 5
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: Toni SalikkaUpdated: Jul 10, 2025Locations: 1
Eligibility criteria

Adult women (18 years or older), assigned female at birth and self-identify as w... [+7]

Presence of severe mental health disorders (e.g., schizophrenia, bipolar disorde... [+4]

Status: Not yet recruiting

Temporal Dynamics of Mindfulness Intervention for Emotional Distress: Daily Interventions and Assessments

This research aims to adopt a complex systems perspective to thoroughly examine the impact of online mindfulness interventions on changes in emotional distress, with a particular focus on the mechanisms of action. Through a daily diary study design, the study seeks to reveal the complexity and dynamic characteristics of emotional changes and the underlying mechanisms(i.e. distress tolerance, experiential avoidance, cognition flexibility, and life engagement) throughout the intervention process. This research will enrich the theoretical framework of online mental health intervention and provide empirical evidence for optimizing online intervention strategies.

Participants needed: 100
Trial details
Age: 18-60Biological sex: AllType: InterventionalSponsor: Peking UniversityUpdated: Apr 9, 2025
Eligibility criteria

Subjects with scores greater than 21 on the Kessler Psychological Distress Scale...

Subjects who could not access the Internet. [+4]

Status: Not yet recruiting

Mindfulness Interventions and Emotional Distress: A Daily Study

This study hopes to explore whether the changes in rumination exhibited in Daily Diary mediates the effects of mindfulness intervention on alleviating emotional distress

Participants needed: 120
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Peking UniversityUpdated: Jan 21, 2025
Eligibility criteria

Subjects with scores greater than 21 on the Kessler Psychological Distress Scale...

Subjects who could not access the Internet. [+4]

Status: Not yet recruiting

Mechanisms of Mindfulness Intervention:Rumination Behavioral Experiments

This study hopes to explore whether the changes in rumination exhibited in behavioral experiments mediates the effects of mindfulness intervention on alleviating emotional distress

Participants needed: 160
Trial details
Age: 18-55Biological sex: AllType: InterventionalSponsor: Peking UniversityUpdated: Dec 9, 2024
Eligibility criteria

- Subjects with scores greater than 21 on the Kessler Psychological Distress Sca... [+1]

- Subjects who could not access the Internet; [+4]

Status: Not yet recruiting

Mechanisms of Mindfulness Intervention: Cognitive Flexibility Dose Manipulation

This study hopes to: 1. explore whether an increase in the dosage of cognitive flexibility intervention corresponds to greater effectiveness of mindfulness intervention in alleviating emotional distress. 2. explore whether cognitive flexibility mediates the effects of mindfulness intervention on alleviating emotional distress.

Participants needed: 300
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Peking UniversityUpdated: Oct 1, 2024Locations: 1
Eligibility criteria

- Subjects with scores greater than 21 on the Kessler Psychological Distress Sca... [+1]

- Subjects who could not access the Internet; [+4]

Status: Not yet recruiting

The OPERa Study: Evaluating QoL After Rectal Cancer Surgery

Advances in rectal cancer management have significantly reduced morbidity and mortality. The most commonly performed operation for rectal cancer is restorative proctectomy (RP), leaving up to 70% with long-term bowel dysfunction called Low Anterior Resection Syndrome (LARS). LARS manifests as stool frequency, incontinence and difficult defecation. LARS, along with other functional impairments such as sexual and urinary dysfunction (SUD), can impact quality of life (QoL) and cause emotional distress. High-quality longitudinal data on these sequalae are lacking, leading to variable estimates of their prevalence, risk factors and prognosis. Most studies are European, cross-sectional, lack pre-treatment evaluation and long-term follow-up, and use inconsistent assessment measures. Thus, a North American study that evaluates patients longitudinally from diagnosis will provide quality data to fill this knowledge gap. The main aim of the proposed study is to contribute evidence regarding the impact of LARS, SUD, emotional/financial distress, and patient activation on long-term post-treatment QoL in North American rectal cancer after RP. This multicenter North American, observational, prospective cohort study relies on validated patient reported outcome measures (PROMs) at diagnosis, during and post-treatment. Patients from 20 sites will be recruited over 2 years and followed for 3 years. The primary endpoint is QoL as measured by the European Organization for Research \& Treatment of Cancer QoL questionnaire. We anticipate accrual of 1200 patients. Factors associated with QoL will be explored. Impact of patient activation in relation to functional outcomes on QoL over time will be explored using a difference-in-differences approach. The study involves a multidisciplinary team who will provide expertise in research methodology, nursing, oncology and surgery. The main contributions of this study are 1) provision of reference baseline North American values for important rectal cancer PROMs for clinical and research use, 2) an understanding of the evolution of functional outcomes and QoL post-treatment to counsel patients peri-operatively and throughout survivorship, and 3) to provide the basis for future tailored programs to support rectal cancer survivors.

Participants needed: 1,200
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Jewish General HospitalUpdated: Aug 18, 2022Duration: 3 Years
Eligibility criteria

Patients >18 years with histopathologically confirmed adenocarcinoma of the rect...

Metastatic disease at diagnosis; [+4]