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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03068871
Other study ID # 0841-16-TLV
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 28, 2017
Est. completion date July 23, 2017

Study information

Verified date October 2018
Source Tel-Aviv Sourasky Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

participants will be randomized into one of three groups: 3-session CET intervention, 3-session ACT intervention, or Waiting List group. Each weekly session will last up to 2 hours and 10 participants will be assigned to each group. There will be two cohorts, with 30 participants in each cohort. The Waiting List group will receive the CET intervention after the groups have completed theirs.


Recruitment information / eligibility

Status Completed
Enrollment 45
Est. completion date July 23, 2017
Est. primary completion date July 23, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Tinnitus lasting more than 3 months

- Hebrew speaking

- Use hearing aids if needed

- Signed informed consent

Exclusion Criteria:

Study Design


Related Conditions & MeSH terms


Intervention

Other:
ACT
Psycho-educational group
CET
Psycho-educational group

Locations

Country Name City State
Israel Sourasky Medical Centre Tel-Aviv

Sponsors (1)

Lead Sponsor Collaborator
Tel-Aviv Sourasky Medical Center

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary COPE Coping scale questionnaire Before the intervention (T1) and at the end of intervention (T2-4 weeks after T1), 1 month after end of intervention (T3)
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