Comparison of the Effects of Therapeutic Touch and Patient Education on Postponed Patients

NCT ID: NCT06502132

Last Updated: 2025-02-05

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

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

78 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-07-03

Study Completion Date

2024-12-27

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The aim of this study is to examine the effect of therapeutic touch and patient education on anxiety, pain, satisfaction levels and physiological parameters of patients and to determine patient experiences. The study will be conducted as a mixed method study. In the study, the effects of therapeutic touch and patient education on anxiety, satisfaction, pain levels and physiological parameters will be compared and the results will be compared. At the same time, qualitative statements of patients will be analyzed in depth and quantitative data will be supported.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

The study will be conducted with a nested design mixed method in which qualitative and quantitative methods will be used together with two experimental groups (education and therapeutic touch) and one control group. For the quantitative part, patients who meet the inclusion criteria will be randomized into the experimental and control groups. For randomization, two main groups will be formed as "major" and "minor" according to the degree of operation. The names of these two main groups will be written on two fans. Then both "major" and "minor" groups will be divided into "therapeutic touch group", "patient education group" and "control group". This separation will be done by writing the names of the subgroups on small pieces of paper, and when there is a patient whose surgery is postponed, after determining which main group the patient belongs to according to the degree of operation, a paper will be randomly drawn from the fan by the researcher, and the patient will be admitted to that group according to the subgroup name written on the paper. Only one of the patients lying in the same room will be included in the study to avoid interference. In addition, data will be collected from the patients assigned to all three groups as a result of randomization by using the phenomenological approach method, one of the qualitative research designs, using the face-to-face interview technique. In addition, data will be collected from the patients assigned to all three groups as a result of randomization by using face-to-face interview technique with the phenomenological approach method, one of the qualitative research designs. It is planned to collect qualitative and quantitative data from the same sample. Before collecting the data, the patients will be informed about the study, their written consent will be obtained verbally and digitally with the informed consent form, and then the 21-question Descriptive Characteristics Form will be applied as a conversation with verbal communication method. This process will contribute to the development of communication. Afterwards, the "State-Trait Anxiety Scale" will be applied to the patients in all groups, and qualitative data will be collected from the patients by applying the "Semi-structured Interview Form Before Interventions" prepared by the researcher in addition to the therapeutic touch and patient information groups. Afterwards, the relevant interventions (therapeutic touch or patient education) will be applied to the experimental groups. After the interventions are applied, the patients will be given one hour to rest. Afterwards, the state part of the "State-Trait Anxiety Scale", the "Numerical Proportioning Scale", the "Physiological Parameters Assessment Form" and the "Patient Satisfaction Assessment Form According to Watson Improvement Processes" will be applied to all groups as a post-test. In addition to the experimental groups, the "Semi-structured Interview Form After Interventions" prepared by the researcher will be administered.

Hypotheses of the Research:

H1: Patient education has a positive effect on anxiety in surgical patients whose operations have been postponed.

H2: Patient education has a positive effect on patient satisfaction in surgical patients whose operations have been postponed.

H3: Patient education has a positive effect on pain in surgical patients whose operations have been postponed.

H4: Patient education has a positive effect on physiological parameters in surgical patients whose operations have been postponed.

H5: Therapeutic touch has a positive effect on anxiety in surgical patients whose operations have been postponed.

H6: Therapeutic touch has a positive effect on patient satisfaction in surgical patients whose operations have been postponed.

H7: Therapeutic touch has a positive effect on pain in surgical patients whose operations have been postponed.

H8: Therapeutic touch has a positive effect on physiological parameters in surgical patients whose operations have been postponed Mixed Methods Research Question: How do the findings obtained through quantitative methods regarding the postponement process in surgical patients whose operations have been postponed correspond to the individual interview data conducted to explore the patients' feelings, thoughts, and experiences regarding the postponement process?

Qualitative Research Method Questions:

1\) What are the feelings and thoughts of surgical patients whose operations have been postponed regarding the postponement situation? 2) What are the experiences of surgical patients whose operations have been postponed regarding the waiting process? 3) What is the relationship between the postponement of the operation and the anxiety, pain and satisfaction levels of the patients in surgical patients whose operations have been postponed? 4) What are the feelings and thoughts of surgical patients whose operations have been postponed regarding the interventions applied during the waiting process? 5) What are the experiences of surgical patients whose operations have been postponed regarding the interventions applied during the waiting process? 6) What are the expectations of surgical patients whose operations have been postponed from physicians and nurses during the waiting process? The study was planned to be conducted with 78 patients as a result of the power analysis test.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Surgery

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Three groups with two experimental groups and one control group, including patient education and therapeutic touch
Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Control Group

Control group patients will receive routine care and no other intervention will be made within the scope of the study.

Group Type NO_INTERVENTION

No interventions assigned to this group

Patient Education Group

The patient education group will be informed about the waiting process that occurs as a result of surgery postponement through an education booklet prepared by the researcher in line with the literature.

Group Type ACTIVE_COMPARATOR

Patient Education Group

Intervention Type OTHER

Patients whose surgery has been postponed will be educated by the researcher through a booklet regarding the waiting process. The education includes information such as anxiety management, pain management, and re-surgery planning. The booklet consists of 22 pages and a copy is given to each patient in this group. The education lasts between 15-20 minutes and the patients' questions are answered. It is applied in a single session.

Therapeutic Touch Group

During the waiting period, patients will receive therapeutic touch by a certified researcher.

Group Type ACTIVE_COMPARATOR

Therapeutic Touch Group

Intervention Type OTHER

Therapeutic touch application is applied as a single session and lasts approximately 20-25 minutes. The therapeutic touch that emerges from the artistic aspect of nursing is an energybased practice that does not involve physical contact. Therapeutic touch is a conscious and compassionate effort to direct the flow of one's universal life energy to healing by influencing this energy.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Patient Education Group

Patients whose surgery has been postponed will be educated by the researcher through a booklet regarding the waiting process. The education includes information such as anxiety management, pain management, and re-surgery planning. The booklet consists of 22 pages and a copy is given to each patient in this group. The education lasts between 15-20 minutes and the patients' questions are answered. It is applied in a single session.

Intervention Type OTHER

Therapeutic Touch Group

Therapeutic touch application is applied as a single session and lasts approximately 20-25 minutes. The therapeutic touch that emerges from the artistic aspect of nursing is an energybased practice that does not involve physical contact. Therapeutic touch is a conscious and compassionate effort to direct the flow of one's universal life energy to healing by influencing this energy.

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Be 18 years of age or olde
* To undergo surgery
* Postponement of the operation for 24 hours
* Being able to read, write and communicate in Turkish
* Not having any vision, hearing or speech problems
* Volunteering to participate in the study

Exclusion Criteria

* Being under 18 years of age
* Complete cancellation of the operation
* Postponing the operation for more than 24 hours
* Having vision, hearing or speech problems that prevent communication
Minimum Eligible Age

18 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Ataturk University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Mehmet Gunay Uyar

Lecturer

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Ataturk University Health Sciences Institute

Erzurum, Yakutiye, Turkey (Türkiye)

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Turkey (Türkiye)

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

AtaturkU-SBE-MGU-01

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

7E Model in Nursing Education
NCT06689306 NOT_YET_RECRUITING NA