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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05708872
Other study ID # NIOCHIR 01/22
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date October 1, 2022
Est. completion date December 2024

Study information

Verified date December 2022
Source Maria Sklodowska-Curie National Research Institute of Oncology
Contact Marta Nowak-Kulpa
Phone +48 322788417
Email Marta.Nowak-Kulpa@io.gliwice.pl
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In this study, it will be investigated whether the methods of self-regulation of mental state have an effect on postoperative pain perception in colon cancer patients.


Description:

According to the assumptions of psychoneuroimmunology, the improvement of mental state affects the physical improvement of patients. Numerous studies confirm the effectiveness of hypnosis and learning autohypnosis in improving the functioning of patients in terms of reducing pain and anxiety, improving the quality of sleep and mood. The study is a Prospective Randomized Controlled Trial consisting of two groups. Patients in the study group will receive a voice recording with hypnotic instructions with a suggestion to improve the psychophysical state. Patients in the control group will receive a recording with relaxing music. Depending on the randomization, patients will listen to the selected recording before being admitted to the surgical department. They will then be given a recording to listen to whenever they want. The patients will be examined four times using the Activity Change Scale, ie. before randomization, on the first day after surgery, on the 7th day after surgery and 1 month after surgery. Simultaneously the total analgesic consumption will be recorded.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date December 2024
Est. primary completion date December 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. Written informed consent to participate in the study 2. Age >= 18 years 3. Histopathological diagnosis of primary colon cancer without distant metastasis 4. Planned surgical treatment 5. Fluency in Polish Exclusion Criteria: 1. Severe comorbidities with pain disorders 2. Regular use of analgesics 3. Coexistence of another neoplastic disease 4. Use of non-pharmacological pain management (including autohypnosis) prior to the study 5. Poor general condition 6. Previous colorectal surgery 7. Hearing disorders 8. No possibility of playback of the received recording

Study Design


Intervention

Behavioral:
Autohypnosis
Patients in the study group will receive a voice recording with hypnotic instructions with a suggestion to improve the psychophysical state.
Relaxing music
Patients in the control group will receive a recording with relaxing music

Locations

Country Name City State
Poland Maria Sklodowska-Curie National Research Institute of Oncology, Gliwice Branch Gliwice

Sponsors (1)

Lead Sponsor Collaborator
Maria Sklodowska-Curie National Research Institute of Oncology

Country where clinical trial is conducted

Poland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Effect of methods of self-regulation of mental state on postoperative pain perception changes The timing of primary outcome measurement includes more than one time point because outcome measurements assess changes in patient status.
The patient's condition will be assessed before surgery and at the following post-operative periods: the first day, the fourth day and one month after surgery. The measure will assess the condition over the last 24 hours on scales ranging from -10 to +10 of the Activity Change Scale.
For pain, the score will be reviewed by asking:
1. Which bodily sensations predominate at the site of the illness? A score of -10 indicates maximal relief; 0 neutral condition; and +10 indicates maximal pain.
For all answers, higher scores mean a worse outcome.
The patient's condition will be assessed before surgery and at the following post-operative periods: the first day, the fourth day and one month after surgery.
Secondary Effect of methods of self-regulation of mental state on mood changes The timing of secondary outcome measurement includes more than one time point because outcome measurements assess changes in patient status.
The patient's condition will be assessed before surgery and at the following post-operative periods: the first day, the fourth day and one month after surgery. The measure will assess the condition over the last 24 hours on scales ranging from -10 to +10 of the Activity Change Scale.
In terms of mood, the grade will be assessed using the following questions:
1. What mood is prevalent? A score of -10 means a maximal increase in mood; 0 state as usual (no change); and +10 means maximal state lowered.
For all answers, higher scores mean a worse outcome.
The patient's condition will be assessed before surgery and at the following post-operative periods: the first day, the fourth day and one month after surgery.
Secondary Effect of methods of self-regulation of mental state on anxiety changes The timing of secondary outcome measurement includes more than one time point because outcome measurements assess changes in patient status.
The patient's condition will be assessed before surgery and at the following post-operative periods: the first day, the fourth day and one month after surgery. The measure will assess the condition over the last 24 hours on scales ranging from -10 to +10 of the Activity Change Scale.
In terms of anxiety, the grade will be assessed using the following questions:
What is the level of anxiety? A score of -10 means maximal calm; 0 state as usual (no change); and +10 means maximal high anxiety.
How do you feel about the future? A score of -10 means maximum hope that things are going to work out; 0 status as usual (no change); and +10 means maximum anxiety about the future.
For all answers, higher scores mean a worse outcome.
The patient's condition will be assessed before surgery and at the following post-operative periods: the first day, the fourth day and one month after surgery.
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