Cataract Online Refraction Evaluation: A Multi Center Randomized Controlled Trial (CORE-RCT)
Primary Purpose
Cataract
Status
Active
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
remote monitoring after cataract surgery
Sponsored by
About this trial
This is an interventional other trial for Cataract focused on measuring e-health, digital, remote monitoring
Eligibility Criteria
Inclusion Criteria:
- Planned for bilateral phacoemulsification cataract extraction and intra-ocular lens implantation (either sequentialor in one procedure)
- ≥ 18 years of age
- No other current ophthalmic conditions or history that negatively influence post-operative visual acuity
- Be able to fill out the health questionnaires (in Dutch, German or English) and perform the web-based refractiveassessment (possibly with assistance of family member or other close relative).
- Specific digital requirements include access to a computer and a smartphone and knowledge how to log in to anonline patient portal.
Exclusion Criteria:
- Cataract extraction surgery combined with other procedures, including: keratoplasty, vitrectomy, glaucoma filter implants
- Ocular comorbidities that negatively influence post-operative visual acuity
- No access to the digital requirements to take the online health questionnaire and/or perform the online refraction.
- Insufficient command of the Dutch, German or English language to understand the questionnaires andinstructions of the web-based refractive assessment or no family member / close relative to assist with this
- Inability of performing the web-based eye exam prior to cataract surgery.
Sites / Locations
- Vienna Institute for Research in Ocular Surgery, Austria
- Augenklink Sulzbach
- Amphia Ziekenhuis
- Oogcentrum Noordholland
- Maastricht UMC+
- Janneau Claessens
Arms of the Study
Arm 1
Arm 2
Arm Type
Other
No Intervention
Arm Label
Telemonitoring
Usual care
Arm Description
Subjects in the telemonitoring group will have post-operative follow-up measurements involving teleconsultations, remote eye exams and health questionnaires.
Subjects in the usual care group will receive regular post-operative care, mostly involving in-hospital consultations.
Outcomes
Primary Outcome Measures
Cost-effectiveness
The main outcome measure will be Incremental cost-effectiveness ratio (ICER), defined as euros per QALY, and compared between the two groups.
Secondary Outcome Measures
Corrected distance visual acuity at the final post-operative visit (achieved with web-based vs manifest refraction)
The corrected distance visual acuity achieved with the web-based refraction will be compared to the corrected distance visual acuity that is achieved with the subjective refraction.
Uncorrected distance visual acuity (web-based vs reference chart)
The uncorrected distance visual acuity that is assessed in the web-based assessment will be compared to the uncorrected distance visual acuity that is assessed using the reference chart.
Refractive error in sphere/cylinder/axes (web-based vs reference chart)
The refractive error (in sphere/cylinder/axes) will be asssessed by the web-based assessment and compared to the subjective refractive error assessment.
Patient reported outcomes
The PROMs questionnaire (CatQuest-9SF) assesses the patient's own reported visual disability from cataract and the improvement after surgery. High scores represent better visual acuity. The results of the PROMs questionnaire will be compared between the groups to assess differences and determine if a web-based follow-up strategy influences these subjective measures. PROMs will be offered in Dutch, German or English accordingly and assessed at baseline and at 3 months follow-up.
Adverse events / additional consultations
All unplanned additional consultations (telephone or hospital) will be recorded. We will count these and compare the frequencies between the two groups.
Total costs
Total costs (in euros) will be determined for both groups. We will count costs for hospital resources and staff, as well as costs for the patient (such as travel and parking costs).
QALY's
To determine the QALY, patients of both groups will be requested to fill out questionnaires to assess quality of life (EQ-5D). A unique health state is defined by combining one level from each of the five dimensions. Higher levels indicate more problems.
Full Information
NCT ID
NCT04809402
First Posted
March 10, 2021
Last Updated
May 31, 2023
Sponsor
UMC Utrecht
Collaborators
Health Holland
1. Study Identification
Unique Protocol Identification Number
NCT04809402
Brief Title
Cataract Online Refraction Evaluation: A Multi Center Randomized Controlled Trial
Acronym
CORE-RCT
Official Title
Cataract Online Refraction Evaluation: A Multi Center Randomized Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
May 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
April 19, 2021 (Actual)
Primary Completion Date
May 10, 2023 (Actual)
Study Completion Date
July 22, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
UMC Utrecht
Collaborators
Health Holland
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
Background of the study:
Cataract is widely prevalent in especially elderly and cataract extraction surgery has thus become one of the most performedsurgeries worldwide. In recent decades the safety of cataract surgery has greatly improved and it is considered one of the safestsurgeries to be performed. Postoperative management consists of routine examinations within one week, to ascertain no adverseevents have occurred immediately after surgery, and between 4-6 weeks, to determine the refractive error. The incidence of seriousadverse events following cataract surgery is estimated to be 1%. As a result, the majority of patient visits after cataract surgery willbe uneventful. Nonetheless valuable time and hospital resources are consumed. Remote monitoring could replace clinicalexaminations in selected patient groups. However, this practice of digital remote monitoring which the patient can use independentlyhas not been clinically validated yet.
Objective of the study:
To determine non-inferiority of the corrected distance visual acuity (CDVA) with the prescription obtained through the web-basedmeasurement of refractive error, compared to usual care, in patients who underwent routine cataract surgery.
Study design:
Observational randomized trial without interventions
Study population:
Patients eligible for cataract surgery, without visual acuity influencing comorbidities or predisposing complicating factors.
Primary study parameters/outcome of the study:
costeffectiveness
Secundary study parameters/outcome of the study (if applicable):
Corrected distance visual acuity at the final post-operative visit, uncorrected distance visual acuity, refractive error(sphere/cylinder/axes), patient reported outcome measurements, adverse events.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cataract
Keywords
e-health, digital, remote monitoring
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
94 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Telemonitoring
Arm Type
Other
Arm Description
Subjects in the telemonitoring group will have post-operative follow-up measurements involving teleconsultations, remote eye exams and health questionnaires.
Arm Title
Usual care
Arm Type
No Intervention
Arm Description
Subjects in the usual care group will receive regular post-operative care, mostly involving in-hospital consultations.
Intervention Type
Other
Intervention Name(s)
remote monitoring after cataract surgery
Intervention Description
remote monitoring after cataract surgery
Primary Outcome Measure Information:
Title
Cost-effectiveness
Description
The main outcome measure will be Incremental cost-effectiveness ratio (ICER), defined as euros per QALY, and compared between the two groups.
Time Frame
pre-operative until 3 months after surgery
Secondary Outcome Measure Information:
Title
Corrected distance visual acuity at the final post-operative visit (achieved with web-based vs manifest refraction)
Description
The corrected distance visual acuity achieved with the web-based refraction will be compared to the corrected distance visual acuity that is achieved with the subjective refraction.
Time Frame
4-6 weeks after surgery
Title
Uncorrected distance visual acuity (web-based vs reference chart)
Description
The uncorrected distance visual acuity that is assessed in the web-based assessment will be compared to the uncorrected distance visual acuity that is assessed using the reference chart.
Time Frame
pre-operative, 4-6 weeks after surgery
Title
Refractive error in sphere/cylinder/axes (web-based vs reference chart)
Description
The refractive error (in sphere/cylinder/axes) will be asssessed by the web-based assessment and compared to the subjective refractive error assessment.
Time Frame
4-6 weeks after surgery
Title
Patient reported outcomes
Description
The PROMs questionnaire (CatQuest-9SF) assesses the patient's own reported visual disability from cataract and the improvement after surgery. High scores represent better visual acuity. The results of the PROMs questionnaire will be compared between the groups to assess differences and determine if a web-based follow-up strategy influences these subjective measures. PROMs will be offered in Dutch, German or English accordingly and assessed at baseline and at 3 months follow-up.
Time Frame
pre-operative vs 3 months after surgery
Title
Adverse events / additional consultations
Description
All unplanned additional consultations (telephone or hospital) will be recorded. We will count these and compare the frequencies between the two groups.
Time Frame
pre-operative until 3 months after surgery
Title
Total costs
Description
Total costs (in euros) will be determined for both groups. We will count costs for hospital resources and staff, as well as costs for the patient (such as travel and parking costs).
Time Frame
pre-operative until 3 months after surgery
Title
QALY's
Description
To determine the QALY, patients of both groups will be requested to fill out questionnaires to assess quality of life (EQ-5D). A unique health state is defined by combining one level from each of the five dimensions. Higher levels indicate more problems.
Time Frame
pre-operative and 3 months after surgery
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Planned for bilateral phacoemulsification cataract extraction and intra-ocular lens implantation (either sequentialor in one procedure)
≥ 18 years of age
No other current ophthalmic conditions or history that negatively influence post-operative visual acuity
Be able to fill out the health questionnaires (in Dutch, German or English) and perform the web-based refractiveassessment (possibly with assistance of family member or other close relative).
Specific digital requirements include access to a computer and a smartphone and knowledge how to log in to anonline patient portal.
Exclusion Criteria:
Cataract extraction surgery combined with other procedures, including: keratoplasty, vitrectomy, glaucoma filter implants
Ocular comorbidities that negatively influence post-operative visual acuity
No access to the digital requirements to take the online health questionnaire and/or perform the online refraction.
Insufficient command of the Dutch, German or English language to understand the questionnaires andinstructions of the web-based refractive assessment or no family member / close relative to assist with this
Inability of performing the web-based eye exam prior to cataract surgery.
Facility Information:
Facility Name
Vienna Institute for Research in Ocular Surgery, Austria
City
Vienna
Country
Austria
Facility Name
Augenklink Sulzbach
City
Sulzbach
Country
Germany
Facility Name
Amphia Ziekenhuis
City
Breda
State/Province
Noord-Brabant
ZIP/Postal Code
4818CK
Country
Netherlands
Facility Name
Oogcentrum Noordholland
City
Heerhugowaard
State/Province
Noord-Holland
ZIP/Postal Code
1704 AG
Country
Netherlands
Facility Name
Maastricht UMC+
City
Maastricht
Country
Netherlands
Facility Name
Janneau Claessens
City
Utrecht
ZIP/Postal Code
3508 GA
Country
Netherlands
12. IPD Sharing Statement
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Cataract Online Refraction Evaluation: A Multi Center Randomized Controlled Trial
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