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The Effect of Reiki on the Anxiety Level of Mothers

O

Ondokuz Mayıs University

Status

Completed

Conditions

Anxiety

Treatments

Other: placebo reiki
Other: reiki

Study type

Interventional

Funder types

Other

Identifiers

NCT06487182
2022/292

Details and patient eligibility

About

The aim of this study is to determine the effect of Reiki applied to mothers whose children were treated in the hospital on the anxiety level.

Full description

Hypotheses 01; there was no difference between the anxiety score of the reiki group and the anxiety score of the control group.

The study will be carried out in three different groups. The practice will start with meeting the women whose children were treated in the hospital. After the women are evaluated in terms of eligibility criteria for the research, the women who are eligible will be informed about the research and written informed consent will be obtained from the women who accept. The random distribution of women to the study groups will be carried out using the Block Randomization method. The following applications will be made to the groups.

Reiki Group The intervention will be applied to the reiki group to be applied in the hospital room. Reiki therapy will be applied by a practitioner with a Reiki application certificate in the application laboratory for 30 minutes while the participants lie down with their eyes closed. 4 sessions of reiki application will be applied to the intervention group for a week. Anxiety level after 4 sessions will be recorded.

Placebo Reiki will be applied to the participants in the group in the application hospital room. The practice will be carried out in the application laboratory for 30 minutes, with the participants sitting with their eyes closed. Reiki life energy will not be transferred to participants in the placebo reiki group. Since the participants' eyes are closed, they will not know that there is a transfer. Placebo Reiki application will be performed in the room 4 times during a week. Placebo application will start, and the first anxiety scores will be recorded. After 4 sessions, anxiety scores will be recorded.

control group; the first anxiety scores will be recorded. After a week later anxiety scores will be recorded.

Enrollment

120 patients

Sex

Female

Ages

18 to 60 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • At least the 3rd day of hospitalization

    • Their child has an acute or chronic disease
    • Able to speak and write Turkish and have no communication problems
    • No psychiatric history and not using medication
    • Not drinking alcohol in the last 24 hours
    • Those who have not received body-mind therapy (yoga, reiki, massage, meditation) in the last six months
    • Mothers who volunteer to participate in the research will be included.

Exclusion criteria

Reiki practitioner or who also has an instructor

  • Having time and communication problems that cannot answer the questions asked
  • Mothers who do not volunteer to participate in the study will not be included in the study.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

120 participants in 3 patient groups

Reiki
Experimental group
Description:
The intervention will be applied to the reiki group in the application hospital room. Reiki therapy will be applied by a practitioner with a Reiki application certificate in the application laboratory for 30 minutes while the participants lie down with their eyes closed. 4 sessions of reiki application will be applied to the intervention group for a week. Reiki application will start , the first anxiety scores will be recorded. Anxiety levels after 4 sessions will be recorded.
Treatment:
Other: reiki
Placebo reiki
Sham Comparator group
Description:
Placebo Reiki will be applied to the participants in the group in the application hospital room. The practice will be carried out in the application room for 30 minutes, with the participants sitting with their eyes closed. Reiki life energy will not be transferred to participants in the placebo reiki group. Since the participants' eyes are closed, they will not know that there is a transfer. Placebo Reiki application will be performed in the room 4 times during a week. Placebo application will start and the anxiety scores will be recorded. After 4 sessions, anxiety scores will be recorded.
Treatment:
Other: placebo reiki
control
No Intervention group
Description:
Routine hospital procedure will be applied. Anxiety scores will be recorded. After a week anxiety scores will be recorded.

Trial contacts and locations

1

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Central trial contact

Sümeyye BAL, Ph.D.; Sümeyye BAL, Ph.D

Data sourced from clinicaltrials.gov

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