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Patient Anxiety During Radiological Examination

Phase 2
Completed
Conditions
Anxiety
Registration Number
NCT02496533
Lead Sponsor
Midwestern Regional Medical Center
Brief Summary

This clinical trial design evaluates whether hand massage reduces anxiety levels in cancer patients as they undergo radiological examination to evaluate tumor response. Anxiety levels will be investigated before massage, after massage, and following the completion of the radiological exam. The Visual Analog Scale (VAS), a validated anxiety assessment tool, will be used to measure anxiety.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
217
Inclusion Criteria
  • Signed informed consent
  • Age ≥ 18 years
  • Scheduled to undergo radiologic imaging evaluation of a tumor
Exclusion Criteria
  • Known hand injury within 30 days prior to study participation
  • Known pregnancy
  • Mental disability as determined by the treating physician
  • Actively receiving radiation therapy
  • Actively receiving chemotherapy

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Change in Anxiety as Measured by Visual Analog ScaleBaseline and After Imaging

Subjects self-reported their perceived anxiety by marking a visual analog scale (VAS). The VAS covers the range 0 to 10. Higher values indicate greater anxiety (worse outcome). Analysis based on difference reported anxiety score between Baseline and after imaging.

Secondary Outcome Measures
NameTimeMethod
Change in Blood Pressure in mmHgBaseline and After Imaging

A trained clinician will measure and record the subject's blood pressure using standard practices.

Change in Respiration Rate in Breaths Per MinuteBaseline and After Imaging

A trained clinician will measure and record the subject's respiration rate using standard practices.

Change in Pulse RateBaseline and After Imaging

A trained clinician will measure and record the subject's radial pulse rate using standard practices.

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