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Oral Vitamin D Substitution Weekly or Monthly and Adherence

Primary Purpose

Vitamin D Deficiency

Status
Completed
Phase
Phase 4
Locations
Switzerland
Study Type
Interventional
Intervention
Vitamin D: liquid form, start weekly
Vitamin D: liquid form, start monthly
Vitamin D: solid form, start weekly
Vitamin D: solid form, start monthly
Sponsored by
University Hospital, Basel, Switzerland
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Vitamin D Deficiency focused on measuring adherence to medication, electronic monitoring

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • vitamin D deficiency by serum level <50 nmol/l
  • polypharmacy defined as 4 daily medicines or more
  • speaking German or Swiss German

Exclusion Criteria:

  • hypercalcaemia
  • substitution treatment with cholecalciferol in the past 3 months
  • medication intake provided by a third person and not by the patient himself

Sites / Locations

  • Pharmaceutical Care Research Group

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Active Comparator

Active Comparator

Active Comparator

Active Comparator

Arm Label

Vitamin D: liquid form, start weekly

Vitamin D: solid form, start weekly

Vitamin D: liquid form, start monthly

Vitamin D: solid form, start monthly

Arm Description

5'600 IU weekly (1.4 ml oily drops) start for 3 months, will cross-over to 24'000 IU monthly (5 ml alcoholic drops) for the following 3 months.

5'600 IU weekly (1 soft capsule) start for 3 months, will cross-over to 20'000 IU monthly (1 tablet) for the following 3 months.

24'000 IU monthly (5 ml alcoholic drops) start for 3 months, will cross-over to 5'600 IU weekly (1.4 ml oily drops) for the following 3 months.

20'000 IU monthly (1 tablet) start for 3 months, will cross-over to 5'600 IU weekly (1 soft capsule) for the following 3 months.

Outcomes

Primary Outcome Measures

Adherence to medication
Taking adherence: number of dosis taken divided by number of dosis prescribed. Timing adherence: number of dosis taken within a time interval (within 15% of the mean preset intake time) divided by number of dosis prescribed.

Secondary Outcome Measures

Serum level of vitamin D
Level of serum vitamin D compared to baseline value.
Patients preferences
Questionnaire with 5-point Likert scale (from 1=strongly disagree to 5=strongly agree)

Full Information

First Posted
March 23, 2017
Last Updated
February 10, 2020
Sponsor
University Hospital, Basel, Switzerland
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1. Study Identification

Unique Protocol Identification Number
NCT03141593
Brief Title
Oral Vitamin D Substitution Weekly or Monthly and Adherence
Official Title
Oral Vitamin D Substitution Weekly or Monthly - Which Procedure Leads to Highest Adherence? A Prospective Intervention Study in Outpatient Care
Study Type
Interventional

2. Study Status

Record Verification Date
February 2020
Overall Recruitment Status
Completed
Study Start Date
October 9, 2017 (Actual)
Primary Completion Date
October 31, 2018 (Actual)
Study Completion Date
October 31, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Basel, Switzerland

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Vitamin D deficiency (defined as 25(OH)-vitamin D serum level <50 nmol/l) is cured with supplementation by mouth. National guidelines recommend the administration of 800 IU cholecalciferol daily for an effective treatment, especially during the winter (poor sun exposition). Commercially available pharmaceutical forms are liquid in Switzerland (drops) and solid forms in Germany (tablets and capsules). Because therapeutic range of vitamin D3 is wide and toxicity is seldom reached, even after the consumption of 200'000 IU, and because the administration of 8 drops daily is inconvenient, weekly and monthly administrations of the cumulative amount (i.e., 5'600 IU weekly or 24'000 IU monthly) have been investigated. Both administration schedules are therapeutic equivalent. The study aims to investigate which form (liquid or solid) and which schedule (weekly or monthly) procure the highest adherence behavior with outpatients under polypharmacy i.e., with 4 or more medications daily. The investigators will use commercially available Swiss and German products.
Detailed Description
Intervention study in patients with serum vitamin D <50 nmol/l and polypharmacy, defined as ≥4 medicaments/day. Treatment duration: 6 months. Treatment groups are defined as Lm (liquid monthly 24'000 IU); Lw (liquid weekly 5'600 IU); Sm (solid monthly 20'000 IU) and Sw (solid weekly 5'600 IU). Cross-over design with identical form (liquid or solid) and switching frequence, i.e. from weekly to monthly treatment and vice versa, for 3 months each.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Vitamin D Deficiency
Keywords
adherence to medication, electronic monitoring

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Crossover Assignment
Model Description
Patient will be recruited by their general practitioners (GP) and allocated to the GP's form (liquid or solid). Patients will be randomly assigned to start weekly or monthly intake for 3 months, and switch to the other frequence for 3 more months.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
97 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Vitamin D: liquid form, start weekly
Arm Type
Active Comparator
Arm Description
5'600 IU weekly (1.4 ml oily drops) start for 3 months, will cross-over to 24'000 IU monthly (5 ml alcoholic drops) for the following 3 months.
Arm Title
Vitamin D: solid form, start weekly
Arm Type
Active Comparator
Arm Description
5'600 IU weekly (1 soft capsule) start for 3 months, will cross-over to 20'000 IU monthly (1 tablet) for the following 3 months.
Arm Title
Vitamin D: liquid form, start monthly
Arm Type
Active Comparator
Arm Description
24'000 IU monthly (5 ml alcoholic drops) start for 3 months, will cross-over to 5'600 IU weekly (1.4 ml oily drops) for the following 3 months.
Arm Title
Vitamin D: solid form, start monthly
Arm Type
Active Comparator
Arm Description
20'000 IU monthly (1 tablet) start for 3 months, will cross-over to 5'600 IU weekly (1 soft capsule) for the following 3 months.
Intervention Type
Drug
Intervention Name(s)
Vitamin D: liquid form, start weekly
Other Intervention Name(s)
Vitamin D3 Streuli
Intervention Description
Patient will start treatment with weekly schedule, and switch after 3 months to monthly schedule for another 3 months.
Intervention Type
Drug
Intervention Name(s)
Vitamin D: liquid form, start monthly
Other Intervention Name(s)
Vi-De 3 Monatsdosis
Intervention Description
Patient will start treatment with monthly schedule, and switch after 3 months to weekly schedule for another 3 months.
Intervention Type
Drug
Intervention Name(s)
Vitamin D: solid form, start weekly
Other Intervention Name(s)
Dekristolvit D3
Intervention Description
Patient will start treatment with weekly schedule, and switch after 3 months to monthly schedule for another 3 months.
Intervention Type
Drug
Intervention Name(s)
Vitamin D: solid form, start monthly
Other Intervention Name(s)
Dekristol
Intervention Description
Patient will start treatment with monthly schedule, and switch after 3 months to weekly schedule for another 3 months.
Primary Outcome Measure Information:
Title
Adherence to medication
Description
Taking adherence: number of dosis taken divided by number of dosis prescribed. Timing adherence: number of dosis taken within a time interval (within 15% of the mean preset intake time) divided by number of dosis prescribed.
Time Frame
3 months of treatment
Secondary Outcome Measure Information:
Title
Serum level of vitamin D
Description
Level of serum vitamin D compared to baseline value.
Time Frame
3 and 6 months
Title
Patients preferences
Description
Questionnaire with 5-point Likert scale (from 1=strongly disagree to 5=strongly agree)
Time Frame
3 months of treatment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: vitamin D deficiency by serum level <50 nmol/l polypharmacy defined as 4 daily medicines or more speaking German or Swiss German Exclusion Criteria: hypercalcaemia substitution treatment with cholecalciferol in the past 3 months medication intake provided by a third person and not by the patient himself
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kurt E Hersberger, Prof
Organizational Affiliation
University of Basel
Official's Role
Study Director
Facility Information:
Facility Name
Pharmaceutical Care Research Group
City
Basel
ZIP/Postal Code
4056
Country
Switzerland

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
not decided yet

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Oral Vitamin D Substitution Weekly or Monthly and Adherence

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