Effects of Progressive Muscle Relaxation Exercise and Finger Grip Exercise on Stress, Anxiety, Fatigue, Sleep Quality, and Physiological Parameters in Pregnant Women With Preeclampsia
The Effects of Progressive Muscle Relaxation Exercise and Finger Grip Exercise on Stress, Anxiety, Fatigue, Sleep Quality, and Physiological Parameters in Pregnant Women With Preeclampsia
The aim of this study is to examine the effects of progressive muscle relaxation exercise and finger grip exercise on stress, anxiety, sleep quality, fatigue and physiological parameters in preeclamptic pregnant women. It is thought that the study will contribute to the improvement of sleep quality by reducing the stress, anxiety and fatigue levels of pregnant women. In this study, which will examine the effects of stress, anxiety, fatigue, sleep quality and physiological parameters of preeclamptic pregnant women, progressive muscle relaxation exercise and finger grip exercise will be used in the same study. No other study has been found where these two methods were used in the same study and the specified parameters were examined together. It is thought that the results of this study will contribute to the literature.
The basic questions that the study will answer are as follows:
H1: The stress level of preeclamptic pregnant women in the progressive muscle relaxation exercise group is lower than that of the control group.
H2: The anxiety level of preeclamptic pregnant women in the progressive muscle relaxation exercise group is lower than that of the control group.
H3: The fatigue level of preeclamptic pregnant women in the progressive muscle relaxation exercise group is lower than that of the control group.
H4: The sleep quality of preeclamptic pregnant women in the progressive muscle relaxation exercise group is better than that of the control group.
H5: The physiological parameters of preeclamptic pregnant women in the progressive muscle relaxation exercise group are better than that of the control group.
H6: The stress level of preeclamptic pregnant women in the finger grip exercise group is lower than that of the control group.
H7: The anxiety level of preeclamptic pregnant women in the finger grip exercise group is lower than that of the control group.
H8: The fatigue level of preeclamptic pregnant women in the finger grip exercise group is lower than that of the control group.
H9: The sleep quality of preeclamptic pregnant women in the finger grip exercise group is better than the control group.
H10: The physiological parameters of preeclamptic pregnant women in the finger grip exercise group are better than the control group.
H11: The effects of progressive muscle relaxation exercise and finger grip exercise on stress levels are different in preeclamptic pregnant women.
H12: The effects of progressive muscle relaxation exercise and finger grip exercise on anxiety levels are different in preeclamptic pregnant women.
H13: The effects of progressive muscle relaxation exercise and finger grip exercise on fatigue levels are different in preeclamptic pregnant women.
H14: The effects of progressive muscle relaxation exercise and finger grip exercise on sleep quality are different in preeclamptic pregnant women.
H15: The physiological parameters of progressive muscle relaxation exercise and finger grip exercise are different in preeclamptic pregnant women.
Researchers will divide participants into experimental and control groups to examine the effects of progressive muscle relaxation exercise and finger grip exercise on stress, anxiety, sleep quality, fatigue and physiological parameters in pregnant women with preeclampsia. There will be 3 groups in the study.
Group 1: PKGE Group Group 2: Finger Grip Group Group 3: Control Group
Progressive muscle relaxation exercise will be applied to group 1, finger grip exercise will be applied to group 2, and no intervention will be applied to group 3.
The data of the study will be collected with the Perceived Stress Scale, State/Trait Anxiety Scale, Richard-Campbell Sleep Scale, Visual Similarity Scale for Fatigue, Physiological Parameters, VAS Score Average.
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Tipo de estudio
Inscripción (Estimado)
Fase
- No aplica
Contactos y Ubicaciones
Ubicaciones de estudio
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Altinordu
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Ordu, Altinordu, Turquía (Türkiye), 52100
- Ordu Üniversitesi Eğitim ve Araştırma Hastanesi Kadın Doğum ve Çocuk Hastalıkları Hastanesi
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Descripción
Inclusion Criteria:
- 18 years of age or older
- Diagnosed with preeclampsia
- In their 20th week of pregnancy or older
- Know and speak Turkish
- Have at least primary school education
- Have a singleton pregnancy
- Voluntarily and agree to participate in the study will be included in the study.
Exclusion Criteria:
• Pregnant women who have been diagnosed with a mental illness and who have begun labor while the study is ongoing will be excluded..
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Investigación de servicios de salud
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Único
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
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Experimental: Finger Grip Exercise
FINGER GRIP EXERCISE WILL BE APPLIED TO THIS GROUP.
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Fingers are connected to energy channels in the body, the nervous system, and the brain.
Holding specific fingers can help calm the energy channel and brain area associated with the finger.
These finger grips can be performed for oneself or for someone else (Weirich, 2021).
The finger grip technique will be applied to preeclamptic pregnant women in the intensive care unit once for 20 minutes during their day of admission, and post-test data will be collected three hours after the procedure.
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Sin intervención: Control Group
NO INTERVENTION WILL BE MADE TO THIS GROUP.
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Experimental: PKGE Group
PROGRESSIVE MUSCLE RELAXATION EXERCISE WILL BE APPLIED TO THIS GROUP.
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A pre-test will be applied to the progressive muscle relaxation exercise, finger grip and control groups of the study.
The data of the study will be collected 3 hours after the women in the progressive muscle relaxation exercise and finger grip exercise groups do 20 minutes of exercise.
No intervention will be made to the control group.
After the data of the study is collected, a post-test will be applied to both the experimental and control groups.
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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STATISTICAL DIFFERENCES BETWEEN EXPERIMENTAL AND CONTROL GROUPS
Periodo de tiempo: It takes approximately one year to complete the study.
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Frequency of stress, anxiety, and fatigue in pregnant women with preeclampsia.
Definition of sleep quality and variability of physiological parameters.
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It takes approximately one year to complete the study.
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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STATISTICAL DIFFERENCES BETWEEN THE CONTROL GROUP AND THE OTHER TWO GROUPS
Periodo de tiempo: It takes approximately one year to complete the study.
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No intervention will be made to the control group, and the other two groups will be treated. Frequency of stress, anxiety, and fatigue in pregnant women with preeclampsia. Definition of sleep quality and variability of physiological parameters. |
It takes approximately one year to complete the study.
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STATISTICAL DIFFERENCES BETWEEN THE CONTROL GROUP AND THE OTHER TWO GROUPS
Periodo de tiempo: It takes approximately one year to complete the study.
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Frequency of stress, anxiety, and fatigue in pregnant women with preeclampsia.
Definition of sleep quality and variability of physiological parameters.
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It takes approximately one year to complete the study.
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Colaboradores e Investigadores
Patrocinador
Investigadores
- Director de estudio: Nülüfer ERBİL, Prof.Dr, Ordu Üniversitesi Sağlık Bilimleri Fakültesi Dekanlığı
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
Finalización primaria (Estimado)
Finalización del estudio (Estimado)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- 001093483
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Descripción del plan IPD
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
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