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Validation and Cross-Cultural Adaptation of the Romanian Version of Oral Health Impact Profile in Edentulous Adults (ROM-OHIP-ED)

Primary Purpose

Severe Atrophy of the Edentulous Mandible

Status
Completed
Phase
Not Applicable
Locations
Romania
Study Type
Interventional
Intervention
Insertion of two screw type dental implants
Sponsored by
Concordia Dent Srl
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Severe Atrophy of the Edentulous Mandible focused on measuring OHIP-EDENT, VALIDATION, OVERDENTURE, ROMANIAN

Eligibility Criteria

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

Inclusion Criteria:

  • Fully mandibular edentulous patients
  • Complains about the stability of the existing mandibular denture satisfactory from a technical point of view.
  • Acceptance of a mandibular over-denture retained by two endosseous implants.
  • Patients agree to a 5-year follow-up period.

Exclusion Criteria:

  • Insufficient bone volume (height and with) for inserting at least a 10 mm implant (Ø 4,1).
  • Angle class II relationship.
  • Physical severe consideration that will affect the minimal invasive surgical procedure or constitute a hindrance for a 5-year follow-up.
  • History of radiotherapy in the head and neck region.
  • History of pre-prosthetic surgery (including bone graft procedures) or previous oral implants.

Sites / Locations

  • Concordia Dent Clinic

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Active Comparator

Arm Label

Retentive Anchor Group

Magnet Group

Locator Group

Arm Description

23 fully edentulous patients will receive Retentive Anchors (Institute Straumann AG, Basel Switzerland)as retention system for the two implant overdenture.

23 fully edentulous patients will receive Magnets (Institute Straumann AG, Basel Switzerland)as retention system for the two implant overdenture.

23 fully edentulous patients will receive Locator (Institute Straumann AG, Basel Switzerland)as retention system for the two implant overdenture.

Outcomes

Primary Outcome Measures

OHIP-EDENT linguistic and cultural adaptation in Romanian
Steps for validation: linguistic and cultural adaptation of the original instrument to Romanian; pilot study to assess face and content validity; main study to assess the reliability and construct validity. OHIP-EDENT questionnaire includes 19-items addressing masticatory capacity, pleasure of eating, level of comfort, and relationship among others while wearing the prosthesis and detects the impact of oral health in the quality of life of edentulous adults wearing total prosthesis. Response categories:4=very often; 3=fairly often; 2=occasionally; 1=hardly ever; 0=never/don't know.

Secondary Outcome Measures

Evaluation of patient satisfaction with the use of three different systems as retention for implant supported mandibular overdentures.
Patient satisfaction is assessed with the use of OHIP-EDENT questionnaire validated in Romanian language. The questionnaire is administrated initial (before surgery for assessing patient satisfaction with the original denture), after 6 months of implant over-denture insertion (T) and at 1,3 and 5-year follow-up (T1, T3, T5). The means scores will be calculated. Lower scores represents a good perception of the oral conditions, good satisfaction level and good masticatory capacity.

Full Information

First Posted
July 11, 2011
Last Updated
February 2, 2015
Sponsor
Concordia Dent Srl
Collaborators
ITI International Team for Implantology, Switzerland
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1. Study Identification

Unique Protocol Identification Number
NCT01392456
Brief Title
Validation and Cross-Cultural Adaptation of the Romanian Version of Oral Health Impact Profile in Edentulous Adults
Acronym
ROM-OHIP-ED
Official Title
Patient Satisfaction With the Use of Three Different Systems as Retention for Implant Supported Mandibular Overdentures.
Study Type
Interventional

2. Study Status

Record Verification Date
February 2015
Overall Recruitment Status
Completed
Study Start Date
June 2004 (undefined)
Primary Completion Date
September 2010 (Actual)
Study Completion Date
February 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Concordia Dent Srl
Collaborators
ITI International Team for Implantology, Switzerland

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The aim of the study is: To validate the Romanian translation of OHIP-EDENT (Oral Health Impact Profile in Edentulous Adults), the short form of OHIP (Oral Health Impact Profile) developed by Allen and Locker for edentulous adults. The OHIP questionnaire is an efficient instrument for assessment of OHRQoL - Oral Health-Related Quality of Life. To compare satisfaction of 69 fully mandibular edentulous patients rehabilitated with implant-supported overdentures with three different types of retention: Retentive Anchors, Magnets, Locator.
Detailed Description
Fully edentulism can substantially affect oral and general health as well overall quality of life and inappropriate treatment using classical prosthesis may impaired buccal function, increase alveolar bone loss and also is often unsatisfactory for most patients. Implant-retained dentures provide successful long-term outcomes, particularly when used to rehabilitate the edentulous mandible (Assad et al. 2004; Chan et al. 1995; Davis et al. 1999). Results achievable with such prostheses are well known: the degree of stability, chewing efficiency, and ultimately patient satisfaction exceeds the benefits obtained with conventional denture treatment. However few studies have addressed the perception of treatments outcomes by patients and is critically important to determine whether there are meaningful differences based on the type of retention used (Retentive Anchors, Magnets, Locator). OHIP-EDENT (Oral Health Impact Profile in Edentulous Adults), the short form (19 items) of OHIP (Oral Health Impact Profile) detects the impact of oral health in the quality of life of patients who wear total prosthesis and include questions addressing masticatory capacity, pleasure of eating, level of comfort and relationship problems. This questionnaire is validated in several languages but still not available in Romanian. Material and methods Linguistic and cultural adaptation: Because the OHIP EDENT had not previously been used in Romania, it was piloted to assess the face and content validity within the target population. The OHIP EDENT was linguistically and culturally adapted to our setting by using the back translation technique (according to guidelines provided by Beaton et al. 2000) in order to maintain cross-cultural equivalence. In this procedure, translations were independently made by two bilingual persons, who then discussed and produced a consensus Romanian version (T1 and T2 produced T12), which was translated back into English by two professional English translator (one native English) who had never seen the original version (BT1 and BT2 versions). The conceptual equivalence between the original instruments and the back-translated versions was supported by an expert committee (formed by 3 researchers: methodologist, two experts on quality of life studies, and the four translators). The definitive Romanian version was produced after the face and content validity results in the pilot study had been approved by this committee. Pilot study: Ethical approval and specific written consent were obtained from the relevant authorities before the pilot study were started. The pilot study was conducted in a convenience sample (n=35) obtained from mandibular edentulous patients who came to the Dental School, University of Medicine and Pharmacy Bucharest, Romania and Concordia Dent Clinic, Bucharest. Participants were clinically examined according to the WHO (World Health Organization) methodology and completed the pilot OHIP EDENT. The comprehensiveness of the instrument was tested by asking about difficulties in understanding items or frequencies, in order to optimize the face and content validity before the main study. Reproducibility was evaluated by measuring test - retest reliability. Test-retest reliability was calculated using intraclass correlation coefficient (ICC). The sample of 35 respondents fully edentulous was interviewed two weeks after the first interview. Main Study: Patient satisfaction was assessed with the aid of OHIP-EDENT questionnaire validated initial (with the original denture), after 6 months and at 1, 3, 5 years post overdenture insertion.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Severe Atrophy of the Edentulous Mandible
Keywords
OHIP-EDENT, VALIDATION, OVERDENTURE, ROMANIAN

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
69 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Retentive Anchor Group
Arm Type
Active Comparator
Arm Description
23 fully edentulous patients will receive Retentive Anchors (Institute Straumann AG, Basel Switzerland)as retention system for the two implant overdenture.
Arm Title
Magnet Group
Arm Type
Active Comparator
Arm Description
23 fully edentulous patients will receive Magnets (Institute Straumann AG, Basel Switzerland)as retention system for the two implant overdenture.
Arm Title
Locator Group
Arm Type
Active Comparator
Arm Description
23 fully edentulous patients will receive Locator (Institute Straumann AG, Basel Switzerland)as retention system for the two implant overdenture.
Intervention Type
Procedure
Intervention Name(s)
Insertion of two screw type dental implants
Other Intervention Name(s)
Straumann (Institute Straumann AG, Basel, Switzerland)
Intervention Description
Each patient (of the 69 recruited) will receive 2 screw-type Straumann (Institute Straumann AG, Basel, Switzerland) standard implants Ø4.1 mm, with SLA surface in the canine region of the mandible with an interconnecting line approaching parallelism with the terminal mandibular hinge axis, in a 1-stage non-submerged procedure according to a strict protocol (Weingart D and ten Bruggenkate 2000).
Primary Outcome Measure Information:
Title
OHIP-EDENT linguistic and cultural adaptation in Romanian
Description
Steps for validation: linguistic and cultural adaptation of the original instrument to Romanian; pilot study to assess face and content validity; main study to assess the reliability and construct validity. OHIP-EDENT questionnaire includes 19-items addressing masticatory capacity, pleasure of eating, level of comfort, and relationship among others while wearing the prosthesis and detects the impact of oral health in the quality of life of edentulous adults wearing total prosthesis. Response categories:4=very often; 3=fairly often; 2=occasionally; 1=hardly ever; 0=never/don't know.
Time Frame
Two-weeks
Secondary Outcome Measure Information:
Title
Evaluation of patient satisfaction with the use of three different systems as retention for implant supported mandibular overdentures.
Description
Patient satisfaction is assessed with the use of OHIP-EDENT questionnaire validated in Romanian language. The questionnaire is administrated initial (before surgery for assessing patient satisfaction with the original denture), after 6 months of implant over-denture insertion (T) and at 1,3 and 5-year follow-up (T1, T3, T5). The means scores will be calculated. Lower scores represents a good perception of the oral conditions, good satisfaction level and good masticatory capacity.
Time Frame
5 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Fully mandibular edentulous patients Complains about the stability of the existing mandibular denture satisfactory from a technical point of view. Acceptance of a mandibular over-denture retained by two endosseous implants. Patients agree to a 5-year follow-up period. Exclusion Criteria: Insufficient bone volume (height and with) for inserting at least a 10 mm implant (Ø 4,1). Angle class II relationship. Physical severe consideration that will affect the minimal invasive surgical procedure or constitute a hindrance for a 5-year follow-up. History of radiotherapy in the head and neck region. History of pre-prosthetic surgery (including bone graft procedures) or previous oral implants.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
CORINA MARILENA I CRISTACHE, DMD, PhD
Organizational Affiliation
CONCORDIA DENT CLINIC
Official's Role
Principal Investigator
Facility Information:
Facility Name
Concordia Dent Clinic
City
Bucharest
ZIP/Postal Code
041335
Country
Romania

12. IPD Sharing Statement

Citations:
PubMed Identifier
20032605
Citation
Zani SR, Rivaldo EG, Frasca LC, Caye LF. Oral health impact profile and prosthetic condition in edentulous patients rehabilitated with implant-supported overdentures and fixed prostheses. J Oral Sci. 2009 Dec;51(4):535-43. doi: 10.2334/josnusd.51.535.
Results Reference
background
PubMed Identifier
11124735
Citation
Beaton DE, Bombardier C, Guillemin F, Ferraz MB. Guidelines for the process of cross-cultural adaptation of self-report measures. Spine (Phila Pa 1976). 2000 Dec 15;25(24):3186-91. doi: 10.1097/00007632-200012150-00014. No abstract available.
Results Reference
background
PubMed Identifier
15592001
Citation
Assad AS, Abd El-Dayem MA, Badawy MM. Comparison between mainly mucosa-supported and combined mucosa-implant-supported mandibular overdentures. Implant Dent. 2004 Dec;13(4):386-94. doi: 10.1097/01.id.0000144512.43654.08.
Results Reference
background
PubMed Identifier
11168258
Citation
Weingart D, ten Bruggenkate CM. Treatment of fully edentulous patients with ITI implants. Clin Oral Implants Res. 2000;11 Suppl 1:69-82. doi: 10.1034/j.1600-0501.2000.011s1069.x.
Results Reference
background
PubMed Identifier
7495628
Citation
Chan MF, Johnston C, Howell RA, Cawood JI. Prosthetic management of the atrophic mandible using endosseous implants and overdentures: a six year review. Br Dent J. 1995 Nov 11;179(9):329-37. doi: 10.1038/sj.bdj.4808917.
Results Reference
background
PubMed Identifier
10635189
Citation
Davis DM, Packer ME. Mandibular overdentures stabilized by Astra Tech implants with either ball attachments or magnets: 5-year results. Int J Prosthodont. 1999 May-Jun;12(3):222-9.
Results Reference
background
PubMed Identifier
15382775
Citation
Naert I, Alsaadi G, Quirynen M. Prosthetic aspects and patient satisfaction with two-implant-retained mandibular overdentures: a 10-year randomized clinical study. Int J Prosthodont. 2004 Jul-Aug;17(4):401-10.
Results Reference
background

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Validation and Cross-Cultural Adaptation of the Romanian Version of Oral Health Impact Profile in Edentulous Adults

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