The hypothesis is that the Vocational Enablement Protocol (VEP) is effective and cost-effective compared with usual care from a societal perspective.
ID
Bron
Verkorte titel
Aandoening
slechthorendheid, gehoorverlies, hearing impairment, hearingloss
Ondersteuning
VU University Medical Center, Dept. of ENT / Audiology, EMGO+ Institute
P.O. Box 7057, 1007 MB Amsterdam, The Netherlands
T: (+31) 20-4440900 (di-vr)/ (+31) 20-4441709 (ma)
F: (+31) 20-4442033
E: a.gussenhoven@vumc.nl
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
Need for recovery after work (NFR) scale comprised 11 dichotmized items assessing the short term effects of fatigue caused by work activities (Meijman en Van Veldhoven, 1994).
Achtergrond van het onderzoek
A randomized controlled trial will be performed with 80 participants in the control (care as usual) and 80 participants in the treatment group (VEP). KLM, Corus and VU university have confirmed their participation in this study. Also patients of the ENT doctors and occupational physician will recruited in the study. All participants give their informed consent. Outcomes will be measured at baseline and after 3, 6, 9 and 12 months en consist of questionnaires. The participants in the intervention group have to visit the Audiological center of the VUmc.
Country of recruitment: The Netherlands.
Doel van het onderzoek
The hypothesis is that the Vocational Enablement Protocol (VEP) is effective and cost-effective compared with usual care from a societal perspective.
Onderzoeksopzet
Baseline measurement and after 3, 6, 9 and 12 months after randomization.
Onderzoeksproduct en/of interventie
People in the intervention group get the VEP. The VEP comprise a half-day assessment of complex problems at the Audiological Center conducted by a team of professionals from different disciplines: E.N.T. physician, audiologist, occupational physician, social worker, psychologist, speech therapist. The patient's hearing status is assessed using an extensive battery of audiotry tests, including pure-tone and speech audiometry, various Speech-Reception-Treshold (SRT) tests (in quiet, in steady state noise and in fluctuating noise) and -if indicated- a test for localization. To examine aided hearing, a free-field version of the SRT in noise test is also performed.
Furthermore, a semi-structured interview is conducted by the psychologist evaluating the psychosocial history of the person, their specific needs, attitude and expectations and an evaluation of the problems at work from the patient's perspective. Refferal information is taken into account. The interview is attended by the occupational physician of the team to specifically evaluate the work-related problems and to discuss the patient's view on possible solutions and legal issues.
If indicated, the workplace itself is visited and is accoustically examined by conducting a Speech-Transmission-Index (STI) measurement. The STI provides an assessment of the intelligibility of speech in the workplace and verifies whether speech is intelligible for the employee, given the hearing impairment and the acousical conditions. The STI measures the combined effects of background noise and reverberation.
At the end of the session, all test results are examined and considered by the psychologist, specialized occupational physician, and the audiologist and explained to the patient. Here, we identify the (mis)match between the audiotry capacities of the employee and the audiotory demands at the workplace. Possibilities of technical, speech-therapeutic and/or psychosocial interventions are then discussed. We argue that a patient-centered approach (i.e. involving the patient in the problem solving process) is crucial.
People in the control group get the usual care of the general practitioner, Ear-, Nose and Throat doctor or the occupational physician.
Publiek
Sophia E. Kramer
VU University Medical Center, Dept. of ENT / Audiology, EMGO+ Institute
Amsterdam 1007 MB
The Netherlands
+31 (0)20 4440969
se.kramer@vumc.nl
Wetenschappelijk
Sophia E. Kramer
VU University Medical Center, Dept. of ENT / Audiology, EMGO+ Institute
Amsterdam 1007 MB
The Netherlands
+31 (0)20 4440969
se.kramer@vumc.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
1. Diagnosis with hearing impairment (i.e. mean pure-tone hearing loss at 1, 2 and 4 kHZ in best ear >25 dB HL) or a score of ‘insufficient’ or ‘poor’ on the National Hearing Test;
2. Age above 18 years;
3. Able to complete questionnaires written in Dutch language and capable of giving informed consent;
4. Working for at least 8 hours a week;
5. Available for the study for the following 12 months.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
1. Not willing or unable to comply with the study protocol;
2. Those who have already been referred to or passed a VEP in the last year;
3. Those for whom tinnitus is the primary condition affecting the individual;
4. Those who were pregnant.
Opzet
Deelname
Opgevolgd door onderstaande (mogelijk meer actuele) registratie
Geen registraties gevonden.
Andere (mogelijk minder actuele) registraties in dit register
Geen registraties gevonden.
In overige registers
Register | ID |
---|---|
NTR-new | NL2654 |
NTR-old | NTR2782 |
Ander register | ZonMw / VUmc : 50-51415-98-015 / 2011/054; |
ISRCTN | ISRCTN wordt niet meer aangevraagd. |