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Running Title: Standardized Care After Back Surgery

The Effect of a Standardized Care Program on Pain, Disability, and Knowledge Among Postoperative Back Surgery Patients in Erbil

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07459985
Enrollment
70
Registered
2026-03-10
Start date
2024-09-29
Completion date
2025-09-20
Last updated
2026-03-10

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

Conditions

Back Pain, Back Surgery, Disabilities, Pain

Keywords

Back surgery, Standardized care, Pain, Disability, Knowledge, Postoperative outcomes

Brief summary

This study aimed to examine the effectiveness of a standardized care program on pain, disability, and patient knowledge among postoperative back-surgery patients in Erbil, Iraq.

Interventions

BEHAVIORALStandardized Educational Care Program

A structured, standardized educational care program is delivered to patients undergoing lumbar spine surgery. The program includes preoperative and postoperative education on pain management, wound care, early mobilization, activity modification, proper body mechanics, medication adherence, prevention of complications, and discharge instructions. Education is provided verbally and through written materials.

Sponsors

Hawler Medical University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

This is a non-randomized, parallel-group interventional study comparing a standardized educational care program versus routine postoperative care among patients undergoing lumbar spine surgery.

Eligibility

Sex/Gender
ALL
Age
21 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Adults between 18 and 60 years of age, of either sex, scheduled for elective thoracic (T1) to lumbar (L5) spine surgery, able to communicate in Kurdish or Arabic, and capable of providing informed consent. Only those willing to complete all follow-up assessments were enrolled to ensure complete data collection.

Exclusion criteria

* Patients who were admitted for emergency procedures, or had cognitive impairments that could interfere with comprehension of instructions. Additional

Design outcomes

Primary

MeasureTime frameDescription
Change in Pain Intensity ScoreBaseline and 8 weeks postoperativelyPain intensity was measured using the Universal Pain Assessment Tool (0-10 numeric rating scale). Higher scores indicate greater pain severity. The primary endpoint is the change in pain score from baseline (pre-intervention) to 8 weeks postoperatively.

Secondary

MeasureTime frameDescription
Change in Functional Disability ScoreBaseline and 8 weeks postoperativelyFunctional disability assessed using the Oswestry Low Back Disability Questionnaire (0-100 scale). Higher scores indicate greater disability. The outcome is the change from baseline to 8 weeks after surgery.

Countries

Iraq

Contacts

STUDY_DIRECTORVian Afan Naqshbandi, PhD

Hawler Medical University/College of nursing, Erbil, Kurdistan Region, Iraq

STUDY_CHAIRNuraddin Hamad Mhammad, PhD

Hawler Medical University/ College of Medicine, Erbil, Kurdistan Region, Iraq

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 11, 2026