Postoperative PainNCT06327282
the Effect of Preoperative Pain Education by Anesthesia Nurses on Postoperative Pain Among Adult Patients Undergoing Abdominal Surgery
An observational study of Postoperative Pain, run by Chinese PLA General Hospital.
Trial summary
To explore the effects of preoperative pain education on postoperative pain among patients undergoing abdominal surgery. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Postoperative Pain
- What is being tested?
- education on pain and related knowledge
- Type of treatment
- Lifestyle or therapy programme
- How many people
- 116 participants
- Where
- No sites listed yet
- Study dates
- 15 Jun 2024to 4 Apr 2025
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: Adult patients undergoing Abdominal Surgery
Who may be able to join
- voluntary informed consent;
- age older than 18 years
- abdominal surgery under elective general anesthesia
Who cannot join
- Patients taking long-term analgesics (including opioids, non-steroids, etc.)
- Patients with preoperative chronic pain
- Have participated in clinical studies in other projects within 3 months prior to signing the informed consent form
- subjects not considered by the investigator
- subjects refused to participate in the study
About this study
To explore the effects of preoperative pain education on postoperative pain among patients undergoing abdominal surgery.
- Conditions
- Postoperative Pain
- Being tested
- education on pain and related knowledge
- Medical subject headings
- Pain, Postoperative
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
education on pain and related knowledgeBehavioural
Also called pain-related knowledge education
Before surgery, pain related knowledge was educated.
| Study group | Role | What they receive |
|---|---|---|
| Intervention group | Anesthesia nurses carried out pain-related knowledge education. Receives: Behavioral: education on pain and related knowledge | |
| Blank group | Patients who did not receive any knowledge education. |
What is being measured
The primary outcome is the main question the study is designed to answer.
Occurrence of pain
The NRS scale was used to evaluate the scores.
Measured: The first day to the fifth day after surgery.
Secondary outcomes (1)
Mastery of the use of patient-controlled analgesia pump
A series of questions were used to assess patients' mastery of patient-controlled analgesia pump use.
Measured: Day 2 after surgery
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted25 Mar 2024
- Study start15 Jun 2024 (estimated)
- Primary completion1 Jan 2025 (estimated)
- Study completion4 Apr 2025 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Postoperative PainStudies of the same condition, open and under way.
- More trials run by Chinese PLA General HospitalThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 116 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Chinese PLA General Hospital
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Hao Li, Chinese PLA General Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06327282
- Sponsor's protocol ID
- ChinaPLAGHPAIN
- Status last verified
- Apr 2024
- First submitted
- 17 Mar 2024
- Last updated
- 23 May 2024
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 23 May 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- the Effect of Preoperative Pain Education by Anesthesia Nurses on Postoperative Pain Among Adult Patients Undergoing Abdominal Surgery
- ClinicalTrials.gov ID
- NCT06327282
- Acronym / sponsor ID
- ChinaPLAGHPAIN
- Conditions
- Postoperative Pain
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 116 participants (estimated)
- Lead sponsor
- Chinese PLA General HospitalUniversity, hospital or other
- Study start
- 15 Jun 2024 (estimated)
- Primary completion
- 1 Jan 2025 (estimated)
- Study completion
- 4 Apr 2025 (estimated)
- First posted
- 25 Mar 2024 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
To explore the effects of preoperative pain education on postoperative pain among patients undergoing abdominal surgery.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Intervention group | – | Behavioral: education on pain and related knowledgeAnesthesia nurses carried out pain-related knowledge education. |
| Blank group | – | –Patients who did not receive any knowledge education. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Adult patients undergoing Abdominal Surgery
Key inclusion criteria (3 listed)
- voluntary informed consent;
- age older than 18 years
- abdominal surgery under elective general anesthesia
Key exclusion criteria (5 listed)
- Patients taking long-term analgesics (including opioids, non-steroids, etc.)
- Patients with preoperative chronic pain
- Have participated in clinical studies in other projects within 3 months prior to signing the informed consent form
- subjects not considered by the investigator
- subjects refused to participate in the study
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| education on pain and related knowledgeAlso: pain-related knowledge educationBefore surgery, pain related knowledge was educated. | Behavioural | Intervention group |
Primary outcome
Occurrence of pain
Time frame: The first day to the fifth day after surgery.
The NRS scale was used to evaluate the scores.
1 secondary outcome
Mastery of the use of patient-controlled analgesia pump
Time frame: Day 2 after surgery
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 23 May 2024.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
Questions about this trial
What is this clinical trial studying?
An observational study of Postoperative Pain, run by Chinese PLA General Hospital.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 23 May 2024. Status can change between updates, so confirm with the study contact before making plans.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Occurrence of pain (time frame: The first day to the fifth day after surgery.). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 23 May 2024.