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In this thesis study, it is thought that with the guided imagery application to the hospitalized pregnant women, there will be a decrease in their stress levels and an increase in their sleep quality. In our country, there is no study where guided imagery application is used in risky pregnant women. It is thought that new information will be added to the literature as a result of this study. This study will be conducted to determine the effect of guided imagery application on pregnancy stress and sleep quality in risky pregnant women.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Guided imagery group | Experimental | Guided imagery will be applied to risky pregnant women in addition to normal nursing care. |
|
| control group | No Intervention | Only routine nursing care will be provided to risky pregnant women. |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Guided imagery | Behavioral | First meeting: The women will be introduced to the clinic, the purpose of the study will be explained, and a written consent form will be filled out. A Personal Information Form and the "Pregnancy Stress Assessment Scale" (GSDS-36) and the "Richard-Campbell Sleep Scale" will be filled out. After the questionnaires are filled out, the vital signs of the pregnant woman will be measured and then a 15-minute guided imagery video will be shown. The vital signs of the patient will be measured again 10 minutes after the guided imagery video is watched. |
| Measure | Description | Time Frame |
|---|---|---|
| Pregnancy Stress Assessment Scale | Pregnancy Stress Assessment Scale will be implemented to the pregnant women. The degree of anxiety, distress and worry experienced by pregnant women is "definitely not", "mild", "moderate", "serious" or "very serious" and is given on a score ranging from 0 to 4, and the perceived stress levels during pregnancy range from a minimum of 0 to a maximum of 144 points. As the score obtained from the scale increases, it is interpreted that stress increases. | During 5 days after the first meeting with participant |
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Inclusion Criteria:
Exclusion Criteria:
Women who have risky pregnancy will be included, therefore the study is gender based.
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Adana City Training and Research Hospital | Adana | Sariçam | 01330 | Turkey (Türkiye) |
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| ID | Term |
|---|---|
| D007319 | Sleep Initiation and Maintenance Disorders |
| ID | Term |
|---|---|
| D020919 | Sleep Disorders, Intrinsic |
| D020920 | Dyssomnias |
| D012893 | Sleep Wake Disorders |
| D009422 | Nervous System Diseases |
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| ID | Term |
|---|---|
| D019018 | Imagery, Psychotherapy |
| ID | Term |
|---|---|
| D026441 | Mind-Body Therapies |
| D000529 | Complementary Therapies |
| D013812 | Therapeutics |
| D011613 | Psychotherapy |
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Due to the study's nature, masking could not be performed.
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|
| D001523 |
| Mental Disorders |
| D004191 |
| Behavioral Disciplines and Activities |