Qigong Intervention and State Anxiety Levels of Inpatiens
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. |
ClinicalTrials.gov Identifier: NCT06006221 |
Recruitment Status :
Completed
First Posted : August 23, 2023
Last Update Posted : November 3, 2023
|
- Study Details
- Tabular View
- No Results Posted
- Disclaimer
- How to Read a Study Record
Condition or disease | Intervention/treatment | Phase |
---|---|---|
Psychiatric Disorder | Behavioral: Qi-gong relaxation exercise | Not Applicable |
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 70 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Masking: | Single (Participant) |
Primary Purpose: | Supportive Care |
Official Title: | The Effect of Qigong Intervention on State Anxiety Levels of Inpatiens in Psychiatric Wards: A Randomized Controlled Study |
Actual Study Start Date : | August 1, 2023 |
Actual Primary Completion Date : | September 10, 2023 |
Actual Study Completion Date : | October 2, 2023 |
Arm | Intervention/treatment |
---|---|
Experimental: experimental group
After the morning meeting, the initiative group will be given 40 minutes of Qigong relaxation exercise.
|
Behavioral: Qi-gong relaxation exercise
Qi-gong relaxation exercise is a mindfulness-based exercise and is a type of exercise that consists of breathing-compatible body movements and relaxation used to relax the body and mind, reduce stress, distract attention from negative thoughts, accelerate blood flow, and improve emotions. |
No Intervention: control group
No application will be made to the control group. The control group will continue their routine treatment in the clinic.
|
- Personal Information Form [ Time Frame: three month ]The personal information form was created by the researchers and includes demographic information and information about the disease. Demographic information consists of seven questions about age, gender, marital status, educational status, employment status, with whom she lives and whether she has a visitor in the clinic. Information about the disease; It consists of eight questions about psychiatric diagnosis, symptoms of hospitalization, duration of illness, number of hospitalizations, drugs used, whether ECT was applied, whether chemical and isolation practices were applied.
- STAI Anxiety Scale I [ Time Frame: three month ]Developed by Spielberger in 1970, its Turkish version was developed by Öner N et al. The validity and reliability study was carried out by adapting it. It is a likert type scale that measures state anxiety levels with 20 questions. Anxiety level is scored as "(1) not at all, (2) a little, (3) a lot, and (4) completely" in STAI-I. Direct statements on the scale, negative emotions; reversed expressions express positive emotions. Two separate total score weights are calculated for each of the direct and reversed statements. The total score for the reverse statements is subtracted from the total score for the direct statements. A predetermined and unchanging value is added to this number. A constant value of 50 was added to the number obtained for STAI-I. The most recent value indicates the individual's anxiety score. The scores obtained from the scale range from 20 to 80. A high score indicates a high level of anxiety.
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
Ages Eligible for Study: | 18 Years to 67 Years (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- The patient is literate and has no communication barriers
- Being an inpatient in the psychiatry clinic
- Being over 18 years old
- The patient has been oriented to the service (at least 24 hours have passed since his hospitalization)
- Regular participation in qigong practice
Exclusion Criteria:
- The patient has communication difficulties
- Having acute psychotic symptoms
- Patients receiving anxiolytic therapy
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT06006221
Turkey | |
Uskudar University | |
Istanbul, Turkey |
Responsible Party: | Emel Erdeniz Güreş, Research Assistant, Uskudar University |
ClinicalTrials.gov Identifier: | NCT06006221 |
Other Study ID Numbers: |
0000000339492770 |
First Posted: | August 23, 2023 Key Record Dates |
Last Update Posted: | November 3, 2023 |
Last Verified: | November 2023 |
Individual Participant Data (IPD) Sharing Statement: | |
Plan to Share IPD: | No |
Studies a U.S. FDA-regulated Drug Product: | No |
Studies a U.S. FDA-regulated Device Product: | No |
psychiatric service,Qi Gong, nursing |
Mental Disorders Problem Behavior Behavioral Symptoms |