- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07685652
Bowel Preparation Quality Following Video-Based Intervention and Educational Booklet Versus Standard of Care in an Outpatient Setting (PrepVibe)
Bowel Preparation Quality Following Video-Based Intervention and Educational Booklet Versus Standard of Care in an Outpatient Setting: A Single-Center, Endoscopist-Blinded Randomized Controlled Trial
Descripción general del estudio
Estado
Intervención / Tratamiento
Descripción detallada
BACKGROUND AND RATIONALE:
Non-pharmacological factors, especially the modality of patient education, may influence bowel preparation quality, yet are underexplored and likely context-dependent based on local staffing, patient characteristics, and practice norms.
STUDY DESIGN:
Prospective, single-endoscopist-blinded, three-arm randomized controlled trial (RCT) with intention-to-treat (ITT) primary analysis. Allocation 1:1:1 using computer-generated random numbers. Endoscopist and endoscopy nurses are blinded to group assignment; participants cannot be blinded due to the nature of the intervention.
SETTING:
Hospital Sibu Endoscopy Unit, Sarawak, Malaysia. Colonoscopies performed by qualified surgeons or registrars under supervision; all endoscopists undergo refresher training on Boston Bowel Preparation Scale (BBPS) scoring for consistency.
STUDY ARMS (INTERVENTIONS):
Arm A (Control): Usual care. Physician/nurse-delivered verbal instructions plus standard pharmacy instructions for bowel preparation solution (split-dose PEG 3L).
Arm B (Written): Tri-lingual (Malay/English/Chinese), plain-language educational leaflet reviewed by health literacy expert, plus brief verbal explanation. Arm C (Visual): Short, structured instructional videos accessible via smartphone QR code, reviewed by health literacy expert, plus brief verbal explanation.
SAMPLE SIZE AND STATISTICAL ANALYSIS:
N=324 (108 per arm). Primary analysis: Intent-to-treat chi-square test comparing adequate vs inadequate BBPS across three arms. Pairwise comparisons with Bonferroni adjustment. Multivariable logistic regression adjusts for prespecified covariates (age, sex, BMI, diabetes, education, language, constipation, study arm).
PRIMARY OUTCOME:
Adequate versus inadequate bowel preparation on Boston Bowel Preparation Scale (BBPS). Adequate = total ≥6 with all segments ≥2.
SECONDARY OUTCOMES:
Polyp detection rate; cecal intubation and withdrawal times; cancellation and repeat rates; patient tolerance; complications; patient-reported clarity and helpfulness; anxiety (VAS-A); demographic predictors.
Tipo de estudio
Inscripción (Estimado)
Fase
- No aplica
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Prasad Mothayapan, MD
- Número de teléfono: +60-84-343333
- Correo electrónico: mprasad.ge@gmail.com
Ubicaciones de estudio
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Sarawak
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Sibu, Sarawak, Malasia, 96000
- Reclutamiento
- Hospital Sibu
-
-
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Descripción
Inclusion Criteria:
- Age 18 years or older
- Outpatients scheduled for elective colonoscopy at Hospital Sibu Endoscopy Unit
- Ability to provide written informed consent
- Access to smartphone or computer with functional internet connectivity
Exclusion Criteria:
- History of non-compliance with prescribed medical regimens
- Cognitive impairment, dementia, or significant mental health disorder compromising informed consent
- Illiteracy or inability to read materials in provided languages
- Prior colonic resection or colostomy
- Inflammatory Bowel Disease (IBD) or Irritable Bowel Syndrome (IBS)
- Significant physical disability (bed-bound or wheelchair-dependent)
- Contraindication to polyethylene glycol (PEG) bowel preparation
- Severe Chronic Kidney Disease (Stage IV or V; eGFR <15 mL/min/1.73m²)
- Significant cardiac comorbidities (unstable angina, severe heart failure, MI within 6 months)
- Inability or unwillingness to comply with study protocol
- Refusal to provide informed consent
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Cuidados de apoyo
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Doble
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Comparador activo: Usual Care (Verbal Counseling)
Standard physician/nurse-delivered verbal instructions and standard pharmacy information sheet for bowel preparation solution (split-dose PEG 3L, Fortrans) according to hospital protocol.
Timing and dietary guidance aligned with standard of care.
No additional written or visual materials provided.
|
Standard verbal instructions delivered by physician or nurse regarding bowel preparation regimen, timing, dietary restrictions, and what to expect during procedure.
|
|
Experimental: Written Educational Pamphlet
Tri-lingual (Malay, English, Chinese) plain-language educational pamphlet detailing step-by-step bowel preparation instructions, plus brief verbal explanation.
Pamphlet reviewed by health literacy expert prior to use.
Same preparation solution and regimen as Control arm.
|
Structured written educational material in Malay, English, and Chinese languages detailing complete bowel preparation instructions, timing, dietary guidance, what to expect, and troubleshooting tips.
Provided to participant with brief verbal explanation.
|
|
Experimental: Visual Media (QR Code Video)
Short, structured instructional videos accessible via smartphone QR code explaining bowel preparation procedure step-by-step, plus brief verbal explanation.
Videos reviewed by health literacy expert prior to use.
Same preparation solution and regimen as Control arm.
|
Short, professionally produced instructional videos accessible via smartphone QR code link.
Videos present step-by-step bowel preparation instructions, timing, dietary guidance, common concerns, and what to expect during procedure.
Participant scans QR code to access video(s) on their smartphone.
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Adequate Bowel Preparation on Boston Bowel Preparation Scale (BBPS)
Periodo de tiempo: On day of colonoscopy procedure, assessed immediately upon colonoscope insertion before lavage (time point: 0 minutes)
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Primary outcome dichotomized as adequate versus inadequate bowel preparation.
Adequate = total BBPS score ≥6 with all three colon segments (left, transverse, right) scoring ≥2 each (scale 0-3 per segment; range 0-9).
Inadequate = total <6 or any segment <2.
Assessment performed before any bowel cleansing/lavage.
|
On day of colonoscopy procedure, assessed immediately upon colonoscope insertion before lavage (time point: 0 minutes)
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Polyp Detection Rate
Periodo de tiempo: During colonoscopy procedure
|
Proportion of participants with at least one polyp detected during colonoscopy.
Documented as yes/no and number of polyps.
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During colonoscopy procedure
|
|
Cecal Intubation Time
Periodo de tiempo: During colonoscopy procedure
|
Time in minutes from colonoscope insertion to identification of cecal landmarks.
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During colonoscopy procedure
|
|
Colonoscopy Withdrawal Time
Periodo de tiempo: During colonoscopy procedure
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Time in minutes from initiation of scope withdrawal to scope exit at rectum, excluding biopsy/therapeutic time.
|
During colonoscopy procedure
|
|
Procedure Cancellation Rate
Periodo de tiempo: On day of scheduled colonoscopy
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Proportion of participants whose colonoscopy was cancelled and reason for cancellation.
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On day of scheduled colonoscopy
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Repeat Colonoscopy Rate
Periodo de tiempo: Within 6 months of initial colonoscopy
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Proportion requiring repeat colonoscopy due to inadequate initial preparation.
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Within 6 months of initial colonoscopy
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Patient Tolerance to Bowel Preparation
Periodo de tiempo: Pre-procedure on day of colonoscopy
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atient self-reported tolerability using five-point scale: Very Easy, Easy, Neutral, Difficult, Very Difficult.
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Pre-procedure on day of colonoscopy
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Procedure-Related Complications
Periodo de tiempo: During procedure and within 7 days post-procedure
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Occurrence of perforation, bleeding, post-polypectomy syndrome, or other adverse events.
|
During procedure and within 7 days post-procedure
|
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Patient-Reported Clarity of Instructions
Periodo de tiempo: Pre-procedure on day of colonoscopy
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Patient perception of clarity using five-point Likert scale.
Statement: "The instructions were clear."
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Pre-procedure on day of colonoscopy
|
|
Patient Anxiety Assessment
Periodo de tiempo: Pre-procedure on day of colonoscopy
|
Patient self-reported anxiety on Visual Analog Scale for Anxiety (VAS-A), 0-10 scale (0=no anxiety, 10=extremely anxious).
|
Pre-procedure on day of colonoscopy
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Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: Prasad Mothayapan, MD, Hospital Sibu, Malaysia
- Director de estudio: Tiong How Chieng, MD, Hospital Sibu, Malaysia
Publicaciones y enlaces útiles
Enlaces Útiles
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
Finalización primaria (Estimado)
Finalización del estudio (Estimado)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Otros números de identificación del estudio
- RSCH-25-05992-BBX
- NMRR-25-04038-EOB (Identificador de registro: Malaysian National Medical Research Registry)
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Descripción del plan IPD
Información sobre medicamentos y dispositivos, documentos del estudio
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