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Anxiety and Fear of Cancer Before and After Banding Without Resection in Small SET Management (QUALI-BANDING-SET)

Anxiety, Fear of Cancer and Quality of Life Degree Before and After Endoscopic Band Ligation Without Resection in Subepithelial Tumours of the Digestive Tract ≤15-mm Management: a Multicenter Prospective Study

Status
Suspended
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04316000
Enrollment
150
Registered
2020-03-20
Start date
2019-11-22
Completion date
2022-03-31
Last updated
2021-09-08

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

Conditions

Gastrointestinal Subepithelial Tumors

Keywords

Tumourophobia, Anxiety for Cancer, Quality of Life, Cancer Worry Scale (CWS)

Brief summary

To analyze the hypothetical improvement in anxiety degree, quality of life and fear of cancer in patients diagnosed with a small gastrointestinal subeptithelial tumor when opting for the removal of the lesion.

Detailed description

This Quality of Life study is directly related to the BANDING-SET study (NCT03247231), whose main aim is to analyze the effectiveness and safety of endoscopic band ligation without resection in the small gastrointestinal subepithelial tumours management. Using three validated tests (Hospital Anxiety and Depression Scale \[HADS\], Cancer Worry Scale \[CWS\] and European Five-Dimension Quality of Live test \[EuroQol-5D\]) patients are evaluated before and after the endoscopic procedure. Three main groups of patients are presented: * GROUP A, in which the subephitelial tumour is successfully removed \[hypothesis: anxiety and fear of cancer should decrease\]. * GROUP B, in which the subephitelial tumour is not successfully removed due to various reasons (size \>15-mm, not technical success,...) \[hypothesis: anxiety and fear of cancer shuold be similar before-after\]. * GROUP C, in which the subephitelial tumour is not observed or is a benign entity, which does not require further interventions for these patients \[hypothesis: anxiety and fear of cancer should decrease\].

Interventions

OTHERInitial Anxiety and Fear of Cancer Test

Answer to Hospital Anxiety and Depression Scale (HADS), Cancer Worry Scale (CWS) and European Five-Dimension Quality of Live test (EuroQol-5D) before the initial endoscopic procedure.

PROCEDUREEndoscopic band ligation without resection of the subpetihelial tumour.

Correct application of the elastic band in the subepithelial tumor, achieving its removal by self-amputation in the 4-6 weeks endoscopic ultrasonography (EUS) control.

OTHER1-2 Months Anxiety and Fear of Cancer Test

Answer to Hospital Anxiety and Depression Scale (HADS), Cancer Worry Scale (CWS) and European Five-Dimension Quality of Live test (EuroQol-5D) after 1-2 months of the initial endoscopic procedure, knowing whether the tumor has either been removed or not, is a benign entity or has not been observed.

OTHER1 Year Anxiety and Fear of Cancer Test

Answer to Hospital Anxiety and Depression Scale (HADS), Cancer Worry Scale (CWS) and European Five-Dimension Quality of Live test (EuroQol-5D) after 1 year of the initial endoscopic procedure, knowing whether the tumor has either been removed or not.

Sponsors

Francesc Bas-Cutrina
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years

Inclusion criteria

* Age between 18 and 80 years. * Patient able to sign and understand the Informed Consent. * Patient with a previously corroborated diagnosis of a subepithelial tumor (SET) by previous endoscopic ultrasonography (EUS), or possible diagnosis of SET by finding a subepithelial lesion (SEL) in a conventional endoscopy performed that will require a EUS study. * Acceptance by the patient as a candidate of the BANDING-SET study (NCT03247231) of assessment of the effectiveness and safety of band ligation without resection of subepithelial tumors of the digestive tract ≤15-mm, with the prior signing of the Informed Consent of this study. * Patient that understand the concept of the study and will complete all the time frame until the study end

Exclusion criteria

* No Informed Consent. * No BANDING-SET study (NCT03247231) Informed Consent. * Patients with functional diversity, unable to understand the nature and possible consequences of the study. * Patients unable to maintain subsequent follow-up (lack of adherence). * Patients with a life expectancy of less than 12 months.

Design outcomes

Primary

MeasureTime frameDescription
Initial Anxiety degree1-2 monthsAt 1-2 months, number of patients with a total anxiety score of 8 or more points in the Hospital Anxiety and Depression Scale (HADS), anxiety subescale. Hospital Anxiety and Depression Scale (HADS), anxiety subescale, legend: * 0-7 points: Normal. * 8-10 points: Borderline anxiety. * 11-21 points: Anxiety disorder.
Initial Fear of Cancer degree1-2 monthsAt 1-2 months, number of patients with a total fear of cancer score of 11 or more points in the Cancer Worry Scale (CWS). Cancer Worry Scale (CWS) legend: * 6-10 points: Low. * 11-15 points: Moderate. * 16-20 points: High. * 21-24 points: Very high.

Secondary

MeasureTime frameDescription
Long-term Anxiety degree1 yearAt 1 year, number of patients with a total anxiety score of 8 or more points in the Hospital Anxiety and Depression Scale (HADS), anxiety subescale. Hospital Anxiety and Depression Scale (HADS), anxiety subescale, legend: * 0-7 points: Normal. * 8-10 points: Borderline anxiety. * 11-21 points: Anxiety disorder.
Long-term Fear of Cancer degree1 yearAt 1 year, number of patients with a total fear of cancer score of 11 or more points in the Cancer Worry Scale (CWS). Cancer Worry Scale (CWS) legend: * 6-10 points: Low. * 11-15 points: Moderate. * 16-20 points: High. * 21-24 points: Very high.

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026