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Effects of Progressive Muscle Relaxation Exercise and Finger Grip Exercise on Stress, Anxiety, Fatigue, Sleep Quality, and Physiological Parameters in Pregnant Women With Preeclampsia

1 giugno 2026 aggiornato da: Hatice Nur Nefes Pala

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.

Panoramica dello studio

Tipo di studio

Interventistico

Iscrizione (Stimato)

90

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

    • Altinordu
      • Ordu, Altinordu, Turchia (Türkiye), 52100
        • Ordu Üniversitesi Eğitim ve Araştırma Hastanesi Kadın Doğum ve Çocuk Hastalıkları Hastanesi

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

Descrizione

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..

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Ricerca sui servizi sanitari
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Separare

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: 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.
Nessun intervento: Control Group
NO INTERVENTION WILL BE MADE TO THIS GROUP.
Sperimentale: 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.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
STATISTICAL DIFFERENCES BETWEEN EXPERIMENTAL AND CONTROL GROUPS
Lasso di tempo: 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.

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
STATISTICAL DIFFERENCES BETWEEN THE CONTROL GROUP AND THE OTHER TWO GROUPS
Lasso di tempo: 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
Lasso di tempo: 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.

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Investigatori

  • Direttore dello studio: Nülüfer ERBİL, Prof.Dr, Ordu Üniversitesi Sağlık Bilimleri Fakültesi Dekanlığı

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

25 novembre 2025

Completamento primario (Stimato)

25 giugno 2026

Completamento dello studio (Stimato)

25 luglio 2026

Date di iscrizione allo studio

Primo inviato

23 settembre 2025

Primo inviato che soddisfa i criteri di controllo qualità

1 giugno 2026

Primo Inserito (Effettivo)

5 giugno 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

5 giugno 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

1 giugno 2026

Ultimo verificato

1 giugno 2026

Maggiori informazioni

Termini relativi a questo studio

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Descrizione del piano IPD

The study will be conducted on pregnant women, a sensitive group, and data will not be shared with third parties until the study is completed. Following completion, the research results are planned to be published as an article in a reputable journal.

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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