- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT01600495
Transcutaneous Electrical Nerve Stimulation for Pain Relief During the Active Phase of Labor
Effects of Transcutaneous Nerve Electrical Stimulation for Pain Relief in Nulliparous Women in Active Phase of Labor
Studieöversikt
Detaljerad beskrivning
Studietyp
Inskrivning (Faktisk)
Fas
- Fas 4
Kontakter och platser
Studieorter
-
-
São Paulo
-
Ribeirão Preto, São Paulo, Brasilien, 14048-900
- centro de referência para a saúde da mulher Ribeirão Preto
-
-
Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
Tar emot friska volontärer
Kön som är behöriga för studier
Beskrivning
Inclusion Criteria:
- primigravida
- literate
- A single fetus in vertex position
- Low-risk Pregnancy
- From 37 weeks of gestation
- Cervical dilatation between 4 and 5 cm with uterine dynamics normal for this stage
- Labor in early spontaneous
- No use of medications during the study period
- Absence of cognitive or psychiatric problems
- Intact membranes
- No risk factors associated
- Who wish to participate and signed the informed consent
Exclusion Criteria:
- TENS procedure intolerance
- Use of any medication or procedure that promotes pain relief
- Use of pacemaker
Studieplan
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Behandling
- Tilldelning: Randomiserad
- Interventionsmodell: Parallellt uppdrag
- Maskning: Enda
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
---|---|
Experimentell: Experimental TENS
TENS Intervention Group(GIE) used for 30 minutes, during uterine contractions between 4-5 cm
|
Use of Transcutaneous Nerve Electrical Stimulation in the lumbosacral region for 30 continuous minutes in the active phase of labor (4-5 cm).
|
Inget ingripande: control Group
Formed by mothers who will not use EAC to receive the routine procedures of motherhood, but will be monitored and evaluated at the same time in the intervention group.
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Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
---|---|---|
Classification of Pain During Labor by Visual Analogue Scale
Tidsram: 30 minutes
|
To evaluate the Transcutaneous Electrical Nerve Stimulation as a resource for pain relief during the active phase of labor will be used the Visual Analogue Scale. Visual analogue scale (VAS): this scale, represented by a rule, the patient estimated pain on a scale of 100 mm (at one end labeled "no pain" associated with a score of 0 mm and at the other end "worst pain imagined" with a score 100 mm) |
30 minutes
|
Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
---|---|---|
Evaluation of TENS During the Active Phase of Labor Over the Use of Analgesia
Tidsram: 10 hours
|
Consider whether the TENS therapy during the active phase of labor could defer request for analgesia use for pain relief for pregnant women.
The cervical dilation indicates the value in centimeters (0-10) of cervical dilation.
Assessed on admission and during labor by doctors (according to the routine of the institution), as recorded in medical records.
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10 hours
|
Duration From Start of Labor Until Birth
Tidsram: 10 hours
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The length of time of labor, specified number of minutes since the opening of the partograph (early labor) until the birth of the child.
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10 hours
|
Number of Participants Who Were Satisfied With the Presence of a Professional/Physiotherapist During Labor.
Tidsram: 10 hours
|
Simple questionnaire (Questionnaire satisfaction of parturients with comparision with experience in this study) developed for this study with 3 items (yes, no and do not want to answer) to assess satisfaction of mothers in the intervention group and the control group regarding the presence of a professional during the period of study and experience in this work.
|
10 hours
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Samarbetspartners och utredare
Sponsor
Utredare
- Huvudutredare: Alessandra C Marcolin, Professor, Faculty of Medicine of São Paulo University
Publikationer och användbara länkar
Studieavstämningsdatum
Studera stora datum
Studiestart
Primärt slutförande (Faktisk)
Avslutad studie (Faktisk)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Uppskatta)
Uppdateringar av studier
Senaste uppdatering publicerad (Uppskatta)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
Termer relaterade till denna studie
Andra studie-ID-nummer
- FR259137
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