- ICH GCP
- Rejestr badań klinicznych w USA
- Badanie kliniczne NCT07630623
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.
Przegląd badań
Status
Warunki
Interwencja / Leczenie
Typ studiów
Zapisy (Szacowany)
Faza
- Nie dotyczy
Kontakty i lokalizacje
Lokalizacje studiów
-
-
Altinordu
-
Ordu, Altinordu, Turcja (Türkiye), 52100
- Ordu Üniversitesi Eğitim ve Araştırma Hastanesi Kadın Doğum ve Çocuk Hastalıkları Hastanesi
-
-
Kryteria uczestnictwa
Kryteria kwalifikacji
Wiek uprawniający do nauki
- Dorosły
- Starszy dorosły
Akceptuje zdrowych ochotników
Opis
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 studiów
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Badania usług zdrowotnych
- Przydział: Randomizowane
- Model interwencyjny: Przydział równoległy
- Maskowanie: Pojedynczy
Broń i interwencje
Grupa uczestników / Arm |
Interwencja / Leczenie |
|---|---|
|
Eksperymentalny: Finger Grip Exercise
FINGER GRIP EXERCISE WILL BE APPLIED TO THIS GROUP.
|
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.
|
|
Brak interwencji: Control Group
NO INTERVENTION WILL BE MADE TO THIS GROUP.
|
|
|
Eksperymentalny: PKGE Group
PROGRESSIVE MUSCLE RELAXATION EXERCISE WILL BE APPLIED TO THIS GROUP.
|
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.
|
Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
|
STATISTICAL DIFFERENCES BETWEEN EXPERIMENTAL AND CONTROL GROUPS
Ramy czasowe: It takes approximately one year to complete the study.
|
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.
|
Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
|
STATISTICAL DIFFERENCES BETWEEN THE CONTROL GROUP AND THE OTHER TWO GROUPS
Ramy czasowe: It takes approximately one year to complete the study.
|
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.
|
|
STATISTICAL DIFFERENCES BETWEEN THE CONTROL GROUP AND THE OTHER TWO GROUPS
Ramy czasowe: It takes approximately one year to complete the study.
|
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.
|
Współpracownicy i badacze
Sponsor
Śledczy
- Dyrektor Studium: Nülüfer ERBİL, Prof.Dr, Ordu Üniversitesi Sağlık Bilimleri Fakültesi Dekanlığı
Daty zapisu na studia
Główne daty studiów
Rozpoczęcie studiów (Rzeczywisty)
Zakończenie podstawowe (Szacowany)
Ukończenie studiów (Szacowany)
Daty rejestracji na studia
Pierwszy przesłany
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy wysłany (Rzeczywisty)
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia weryfikacja
Więcej informacji
Terminy związane z tym badaniem
Słowa kluczowe
Dodatkowe istotne warunki MeSH
Inne numery identyfikacyjne badania
- 001093483
Plan dla danych uczestnika indywidualnego (IPD)
Planujesz udostępniać dane poszczególnych uczestników (IPD)?
Opis planu IPD
Informacje o lekach i urządzeniach, dokumenty badawcze
Bada produkt leczniczy regulowany przez amerykańską FDA
Bada produkt urządzenia regulowany przez amerykańską FDA
Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .