NCT07231562

Brief Summary

In this study, the researcher will examine the effects of preoperative mobilization training (video viewing with VR glasses and brochure methods) given to patients undergoing surgery in the lumbar region on pain, anxiety, fear of movement, fear of falling, and mobility levels in the postoperative period, using specific scales.

Trial Health

63
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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
2mo left

Started Nov 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress78%
Nov 2025Jul 2026

First Submitted

Initial submission to the registry

October 1, 2025

Completed
1 month until next milestone

Study Start

First participant enrolled

November 1, 2025

Completed
Same day until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2025

Completed
16 days until next milestone

First Posted

Study publicly available on registry

November 17, 2025

Completed
8 months until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2026

Expected
Last Updated

November 17, 2025

Status Verified

November 1, 2025

Enrollment Period

Same day

First QC Date

October 1, 2025

Last Update Submit

November 14, 2025

Conditions

Keywords

Lumbar regionkinesiophobiamobilizationnursing care and educationperioperative period

Outcome Measures

Primary Outcomes (2)

  • Tampa Kinesiophobia Scale (TKS)

    The TSK is a 17-question scale developed to determine the level of injury/re-injury and fear-avoidance processes associated with activities. The scale is scored using a four-point Likert scale: "1 = Strongly Disagree," "2 = Disagree," "3 = Agree," and "4 = Strongly Agree." The minimum score on the scale is 17, while the maximum score is 68.

    eight months

  • Patient Mobility Scale-HHO

    The Patient Mobility Scale consists of eight items and four subscales: turning from side to side in bed, sitting at the edge of the bed, standing at the edge of the bed, and walking in the patient's room. The level of pain and difficulty experienced is assessed using a 15-cm visual analog with verbal statements listed below the scale. The numerical value of the degree of pain and difficulty is determined by measuring the distance between the patient's mark on the scale and "0" using a calibrated ruler (no pain, some pain, moderate pain, a lot of pain, the worst pain I can imagine/very easy, easy, a little difficult, difficult, very difficult). The lowest and highest scores for each item range from 0 to 15, and the total scale score ranges from 0 to 120.

    eight months

Secondary Outcomes (5)

  • Observer Mobility Scale-GHÖ

    eight months

  • Visual Anolog Skala-VAS

    eight months

  • State and Trait Anxiety Scale

    eight months

  • Likert-Type Fear of Falling Scale

    eight months

  • Patient Information Form

    eight months

Study Arms (2)

intervention group

EXPERIMENTAL

A group of 30 patients who will receive training on mobilization by watching videos and brochures using virtual reality glasses during the preoperative period (Intervention group).

Other: The group that will receive mobilization training using virtual reality glasses and brochures

control group

NO INTERVENTION

A group of 30 patients who did not receive any video or brochure training other than the routine mobilization process during the preoperative period, and whose differences were examined and compared with those in the intervention group (control group).N

Interventions

A group of 30 patients who will receive training on mobilization by watching videos and brochures using virtual reality glasses during the preoperative period (Intervention group).

Also known as: the group to be given mobilization training
intervention group

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may not qualify if:

  • Having a neurological (such as dementia/Alzheimer's) or psychiatric (such as schizophrenia) medical diagnosis that affects cognitive status.
  • Having a chronic pain disorder.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Eskişehir Şehir Hastanesi

Eskişehir, Odunpazarı, 26080, Turkey (Türkiye)

Location

Related Links

MeSH Terms

Conditions

DiseaseKinesiophobia

Condition Hierarchy (Ancestors)

Pathologic ProcessesPathological Conditions, Signs and SymptomsPhobic DisordersAnxiety DisordersMental Disorders

Study Officials

  • Oğuz ÖZDEMİR

    Suleyman Demirel University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Oğuz ÖZDEMİR, Graduate Student

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Model Details: an intervention group that would receive mobilization training and a control group that would not receive training.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

October 1, 2025

First Posted

November 17, 2025

Study Start

November 1, 2025

Primary Completion

November 1, 2025

Study Completion (Estimated)

July 1, 2026

Last Updated

November 17, 2025

Record last verified: 2025-11

Data Sharing

IPD Sharing
Will not share

We do not want to share the IPD without any justification.

Locations