NCT06279117

Brief Summary

Aim: This study was planned to determine the effect of therapeutic touch applied to nursing students on test anxiety. Method: Students who met the inclusion criteria were divided into therapeutic touch and control groups using the randomization method. After the groups were determined, the students filled out the Introductory Information Form and the State Exam Anxiety Scale. 30 minutes before the exam, therapeutic touch was applied to each of the students, who were divided into groups, for 20 minutes. No application was made to the control group, and they were told to wait in the classroom where the group was waiting as they wished.Immediately after the application was completed, the scale was re-applied to both groups.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
46

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jan 2024

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 15, 2024

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

February 18, 2024

Completed
8 days until next milestone

First Posted

Study publicly available on registry

February 26, 2024

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 15, 2024

Completed
3 days until next milestone

Study Completion

Last participant's last visit for all outcomes

May 18, 2024

Completed
Last Updated

May 21, 2024

Status Verified

May 1, 2024

Enrollment Period

4 months

First QC Date

February 18, 2024

Last Update Submit

May 20, 2024

Conditions

Keywords

therapeutic touchnursing caretest anxiety

Outcome Measures

Primary Outcomes (2)

  • Text Anxiety

    Comparison of test anxiety results of therapeutic touch group and control group. The students' test anxiety score data were collected by the State Test Anxiety Scale. It is a 22-item scale. The scores in the inventory range from 22 to 88. Higher points show a higher level of anxiety.

    Individuals in the therapeutic touch and control groups will be measured as a baseline before the application.

  • Text Anxiety

    Comparison of test anxiety results of therapeutic touch group and control group. The students' test anxiety score data were collected by the State Test Anxiety Scale. It is a 22-item scale. The scores in the inventory range from 22 to 88. Higher points show a higher level of anxiety.

    After the therapeutic touch is completed, individuals in both groups will be measured again within an average of 10 minutes.

Study Arms (2)

Therapeutic touch group

EXPERIMENTAL

Individuals who undergo therapeutic touch will receive therapeutic touch for 20 minutes 30 minutes before the exam.

Behavioral: therapeutic touch

control group

NO INTERVENTION

No treatment will be performed on individuals in the control group.

Interventions

Individuals who undergo therapeutic touch will receive therapeutic touch for 20 minutes 30 minutes before the exam.

Therapeutic touch group

Eligibility Criteria

Age18 Years - 30 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • To be over 18 years of age,
  • To know Turkish and to agree to participate in the research
  • Being a fourth year nursing student
  • Not having received any energy therapy (reiki, therapeutic touch) before

You may not qualify if:

  • Presence of existing psychiatric illness,
  • Using anxiolytic and antidepressant medications

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Gizem Göktuna

Izmir, 35000, Turkey (Türkiye)

Location

MeSH Terms

Interventions

Therapeutic Touch

Intervention Hierarchy (Ancestors)

Mind-Body TherapiesComplementary TherapiesTherapeuticsSpiritual Therapies

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Model Details: Randomised controlled clinical trial
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

February 18, 2024

First Posted

February 26, 2024

Study Start

January 15, 2024

Primary Completion

May 15, 2024

Study Completion

May 18, 2024

Last Updated

May 21, 2024

Record last verified: 2024-05

Locations