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Guided Imagery on the Perceived Stress Level in High-Risk Pregnancies

NCT ID: NCT05021289

Last Updated: 2021-08-31

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

128 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-02-01

Study Completion Date

2021-05-01

Brief Summary

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This research was conducted to identify the effect of the practice of Guided Imagery on the perceived stress level in high-risk pregnancies.

Detailed Description

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Designed as a prospective randomized single-blind trial, the research was performed with the participation of a total of 128 women who had high-risk pregnancies and received inpatient treatment on 1 February - 1 May 2021 at the perinatology service of a maternity and children's hospital located in the Anatolian side of Istanbul province of Turkey (64 pregnant women in the experimental group, 64 pregnant women in the control group).

Conditions

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High Risk Pregnancy

Keywords

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Guided Imagery Perceived Stress Level High-Risk Pregnancies.

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Designed as a prospective randomized single-blind trial, the research was performed with the participation of a total of 128 women who had high-risk pregnancies and received inpatient treatment on 1 February - 1 May 2021 at the perinatology service of a maternity and children's hospital located in the Anatolian side of Istanbul province of Turkey (64 pregnant women in the experimental group, 64 pregnant women in the control group).
Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

SINGLE

Participants
care provider

Study Groups

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Guided İmagery

• participants were given one session of guided imagery.

Group Type EXPERIMENTAL

guided imagery

Intervention Type BEHAVIORAL

guided imagery

control group

No intervention was applied on the control group patients.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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guided imagery

guided imagery

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Being aged 18 years or above
* Agreeing to participate in the study
* Being literate in Turkish

Exclusion Criteria

* The pregnant women who voluntarily wanted to leave the research at any stage after being included in the study, could not communicate verbally, had a visual or hearing disorder, and were previously diagnosed with a psychiatric disease were excluded from the research
Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Nursel Alp Dal

OTHER

Sponsor Role lead

Responsible Party

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Nursel Alp Dal

Assistant Professor

Responsibility Role SPONSOR_INVESTIGATOR

Locations

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Munzur University

Tunceli, Merkez, Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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MunzurUn

Identifier Type: -

Identifier Source: org_study_id