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Comfort Without Medications: Nurse-Led Ways to Reduce Pain and Anxiety During Drain Removal After Bariatric Surgery

A nurse-led, Non-Pharmacological Interventions for Pain and Anxiety Reduction During Drain Tube Removal among Bariatric Patients: A Randomized Comparative Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250306064953N2
Enrollment
40
Registered
2025-06-02
Start date
2025-03-01
Completion date
Unknown
Last updated
2025-07-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bariatric Surgery. Excessive and redundant skin and subcutaneous tissue

Interventions

Intervention 1: Intervention group: Cold Gel Packs. The cold application technique involves the removal of a drain tube with the use of a cooling gel pack. The researcher will preserve the gel packs i

Sponsors

College of Nursing/University of Baghdad
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Adults aged 18–60 years Underwent bariatric surgery (e.g., sleeve gastrectomy, gastric bypass) with postoperative surgical drain placement. Conscious, oriented, and able to communicate effectively in the language used for interventions and assessments. Drain tube scheduled for removal within 48–72 hours postoperatively. Willing to participate and provide written informed consent. Stable vital signs (as determined by the attending physician/nurse). Pain score =3 on a 0–10 numerical rating scale before the drain removal (to ensure intervention relevance).

Exclusion criteria

Exclusion criteria: Psychiatric or cognitive disorders that interfere with communication, comprehension, or cooperation (e.g., dementia, schizophrenia). Hearing or visual impairments that would hinder the ability to participate in guided meditation or deep breathing instructions. Use of sedatives, opioids, or anxiolytics within 4 hours prior to the drain removal. Postoperative complications (e.g., infection, bleeding, hemodynamic instability) that might require emergency care. Known allergy or intolerance to cold therapy or materials used in gel packs. History of chronic pain conditions or current use of long-term pain management therapy. Participation in another clinical trial that may interfere with this study.

Design outcomes

Primary

MeasureTime frame
Reduction in self-reported pain and anxiety levels during drain tube removal through nurse-led, non-pharmacological interventions in bariatric patients. Timepoint: Twenty minutes Before intervention and immediately after intervention. Method of measurement: Patients will be asked to rate their pain by using the Visual Analogue Scale (0-10) before and immediately after drain tube removal. A lower number (0) indicates no pain; (1-3) indicates mild pain, (4-6) moderate pain, (7-9) severe pain, and (10) indicates the worst pain. Also, anxiety levels will be measured by using a six-item state anxiety scale derived from the State-Trait Anxiety Inventory, which consists of six items only, each item [1: No at all, 2: Somewhat, 3: Moderate So, 4: Very much so] before and immediately after drain tube removal.

Secondary

MeasureTime frame
1. Physiological responses during drain removal. Timepoint: Changes in heart rate, blood pressure, and respiratory rate will be measured before and after the procedure to objectively assess stress and anxiety levels. Method of measurement: sphygmomanometer for blood pressure measurement and pulse oximetry for oxygen saturation.;2. Patient satisfaction with care. Timepoint: before and after intervention. Method of measurement: Assessed using a validated satisfaction scale or Likert-type questionnaire to evaluate patients' perceptions of the nurse-led interventions.;3. Procedure duration. Timepoint: before and after intervention. Method of measurement: Time taken to complete the drain removal, recorded in minutes, to determine whether the interventions affect procedural efficiency.

Countries

Iraq

Contacts

Public ContactAli Malik Tiryag

College of Nursing/University of Baghdad

ali.malik@uobasrah.edu.iq+964 781 173 5332

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026