The Effect of Methods of Self-regulation of Mental State on Pain Perception in the Postoperative Period in Colon Cancer Patients

Sponsor
Maria Sklodowska-Curie National Research Institute of Oncology (Other)
Overall Status
Recruiting
CT.gov ID
NCT05708872
Collaborator
(none)
100
1
2
26
3.8

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Autohypnosis
  • Behavioral: Relaxing music
N/A

Detailed 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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
100 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Care Provider, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
The Effect of Methods of Self-regulation of Mental State on Pain Perception in the Postoperative Period in Colon Cancer Patients
Actual Study Start Date :
Oct 1, 2022
Anticipated Primary Completion Date :
Dec 1, 2024
Anticipated Study Completion Date :
Dec 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Study group

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

Active Comparator: Control group

Behavioral: Relaxing music
Patients in the control group will receive a recording with relaxing music

Outcome Measures

Primary Outcome Measures

  1. Effect of methods of self-regulation of mental state on postoperative pain perception changes [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 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.

Secondary Outcome Measures

  1. Effect of methods of self-regulation of mental state on mood changes [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 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.

  2. Effect of methods of self-regulation of mental state on anxiety changes [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 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.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Maria Skłodowska-Curie National Research Institute of Oncology, Gliwice Branch Gliwice Poland 44-102

Sponsors and Collaborators

  • Maria Sklodowska-Curie National Research Institute of Oncology

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Maria Sklodowska-Curie National Research Institute of Oncology
ClinicalTrials.gov Identifier:
NCT05708872
Other Study ID Numbers:
  • NIOCHIR 01/22
First Posted:
Feb 1, 2023
Last Update Posted:
Feb 1, 2023
Last Verified:
Dec 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Maria Sklodowska-Curie National Research Institute of Oncology
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 1, 2023