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Anxiety clinical trials

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NCT ID: NCT05575349 Completed - Anxiety Clinical Trials

Effects of Mandala Coloring on Anxiety and Quality of Life of Women in the Climacteric Period

Start date: December 12, 2022
Phase: N/A
Study type: Interventional

This research was planned as a randomized controlled experimental study in order to reduce the anxiety felt and improve the quality of life by women in the climacteric period.

NCT ID: NCT05570773 Completed - Anxiety Clinical Trials

Effects of Peer Support and Progressive Relaxation Exercises on Sleep Quality and Anxiety

Start date: February 12, 2021
Phase: N/A
Study type: Interventional

The effect of peer support and progressive relaxation exercise programs on midwifery students' sleep and anxiety levels in the COVID-19 pandemic was investigated in the present research. One hundred and four subjects were found eligible for the study according to the inclusion criteria, and they were grouped into three: the peer support program group (PSP) (n=34), the progressive relaxation exercise group (PRE) (n=35), and control group (n=35). The PRE group was given an online relaxation exercise program. The PSP group was given an online peer support program. The data collection tools included a descriptive data form, State-Trait Anxiety Inventory (STAI-I-II), and Pittsburgh Sleep Quality Index (PSQI). The scores of the groups that they obtained from the pre-test application of the STAI-I and PSQI did not yield a statistically significant difference. The scores that PRE and PSP groups obtained from the post-test application of the STAI-I and PSQI were lower than the score that was obtained by the control group on the post-test application of the measures, and difference was evaluated to be significant. Although the mechanisms of action of these two methods are different, it has been observed that they have similar effects in improving anxiety levels and sleep quality.

NCT ID: NCT05566691 Completed - Anxiety Clinical Trials

Strategies for Coping With Negative Thoughts

Start date: August 29, 2022
Phase: N/A
Study type: Interventional

The primary objective of this study is to assess the impact of two strategies for coping with negative automatic thoughts (positive thinking and cognitive restructuring) on one's belief in negative thoughts and one's affect. Another main objective is to assess whether participating in a positive mood induction (versus no mood induction) prior to using one of the two coping strategies impacts belief in negative thoughts and affect. We will also explore the interaction between strategy condition and mood induction condition. As secondary outcomes, we will evaluate whether there are changes in positive thinking skills and cognitive restructuring skills and depressive symptoms after one week of using the strategy.

NCT ID: NCT05562752 Completed - Anxiety Clinical Trials

Pilot Study to Assess the Effect of a Probiotic Blend on Moderate Self-reported Anxiety.

Anx
Start date: December 20, 2022
Phase: N/A
Study type: Interventional

This study evaluates the efficacy of a multistrain probiotic administered in the form of a capsule in the management of moderate self-reported anxiety in adults aged 18-65

NCT ID: NCT05562739 Completed - Anxiety Clinical Trials

Pilot Study to Assess the Effect of a Postbiotic Blend on Moderate Self-reported Anxiety

Anx
Start date: January 4, 2024
Phase: N/A
Study type: Interventional

This study evaluates the efficacy of a multistrain postbiotic administered in the form of a capsule in the management of moderate self-reported anxiety in adults aged 18-65

NCT ID: NCT05559021 Completed - Depression Clinical Trials

What Concept of Manual Therapy is More Effective?

Start date: October 20, 2022
Phase: N/A
Study type: Interventional

The aim of the study will be to find out which manual therapy approach is most effective for the improvement of symptoms (sensory, cognitive, emotional and social) in people with Fibromyalgia.

NCT ID: NCT05550610 Completed - Pain Clinical Trials

Evaluation of Mindfulness and Yoga in Basic Combat Training

Start date: October 12, 2020
Phase: N/A
Study type: Interventional

The present study is a group randomized trial assessing the impact of mindfulness and yoga training on the health, performance, and well-being of soldiers in Basic Combat Training (BCT). Randomization occurred at the platoon level, and platoons received either a combined mindfulness and yoga regimen or training as usual.

NCT ID: NCT05546216 Completed - Anxiety Clinical Trials

Determination of the Effect of Raised Supine Position and Back Support on Back Pain, Anxiety and Comfort Level in Coronary Angiography Patients

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

In addition to pharmacological methods, non-pharmacological methods are also used to control back pain and anxiety. The aim of the study is to determine the effect of 30 degrees raised supine position and back support applied to patients undergoing coronary angiography from the femoral artery on back pain, anxiety and patient comfort. This research was planned as a pretest-posttest randomized, controlled, experimental study in order to determine the effect of the elevated supine position and back support application applied to patients undergoing coronary angiography with femoral artery access on back pain, anxiety and comfort levels of patients. Research Kahramanmaraş Sütçü İmam University SUAH Hospital Cardiology intensive care unit September 2021 - September The sample of the research was determined by power analysis. According to the calculation made, the sample; With an effect size of 0.90, a margin of error of 0.05, a confidence interval of 0.95, and a power of 0.95, it was calculated that there should be 35 people in each group to represent the universe. "Patient Information Form", "Numeric Pain Intensity Scale VAS", "State- The necessary information of the patient will be collected with the "Trait Anxiety Scale" and the "Immobilization comfort scale". After the information of the patient whose hemodynamics is provided, the experimental group will be given a 30 degrees Elevated Supine Position and the back area will be supported with a 36x33x10 sized silicone gel pad that prevents sweating, and the measurements will be repeated at the 2nd and 4th hours after the CAG procedure. The patients in the control group will have the same measurements at the 0th hour, 2nd hour and 4th hour after the femoral angiography procedure. During this period, the patients will remain in the straight supine position without back support, which is routinely applied in the clinic.

NCT ID: NCT05539820 Completed - Anxiety Clinical Trials

Reiki Effects on the State Test Anxiety Levels and Exam Success

Start date: June 10, 2022
Phase: N/A
Study type: Interventional

This study aimed to determine the effect of distant Reiki on first-year nursing students' state test anxiety levels and exam success.

NCT ID: NCT05538039 Completed - Anxiety Clinical Trials

Reducing Anxiety of Children and Their Parents in the Pre-elective Surgery Process

Start date: September 16, 2022
Phase: N/A
Study type: Interventional

It is emphasized in the studies that the child and parent anxiety that occurs in pediatric surgery should be prevented or reduced. According to previous studies, one way to reduce child and parent anxiety in the preoperative process is distraction interventions the child and family with preoperative family-centered activities. Teaching children anxiety coping skills with the involvement of their parents can reduce preoperative anxiety. This study was planned to Comparison of the effectiveness of two different distraction interventions (distraction with play dough- distraction with kaleidoscope) in reducing preoperative anxiety of children and parents who are scheduled for elective surgery