Effects of Vocational Rehabilitation Group Intervention on Motivation and Occupational Self-Awareness in Individuals With Intellectual Disabilities

Sponsor
Hacettepe University (Other)
Overall Status
Completed
CT.gov ID
NCT04728074
Collaborator
Biruni University (Other)
49
1
2
3.2
15.5

Study Details

Study Description

Brief Summary

This study is an intervention study that investigates the effects of a group-based approach to motivation and occupational self-awareness of individuals with intellectual disability (ID).

The intervention method was developed by following the intervention mapping method.

An 8 weeks group intervention (twice a week) was applied to individuals with ID which includes; Introduction to intervention and meeting with other group members self-awareness training occupational self-awareness taking responsibility group work and labor division problem identification problem-solving

The entire program was structured and guided by the prepared manual (available upon request from the authors). The manual was prepared by the authors of this study to ensure consistency between different sessions and groups. All sessions were diffusively explained in the manual as well as the individual session booklets. The supervisors were able to follow the structure of the sessions from those booklets. Additionally, there were visual materials for each session as in; presentations, graphics, and photographs. The program supervisors (therapists) met once every week to discuss the progress, participation, and overall status of each participant.

Homework assignments were utilized to facilitate learning. Families were not included directly in the group sessions, however were informed about the homework assignments. Homework assignments consisted of very basic mental practice and reenactment regarding the session's topic and concepts. Families were also included in the final week's sessions since graduation certificates were handed out during these sessions and also small celebrations were carried out.

Condition or Disease Intervention/Treatment Phase
  • Other: The Entering Employment and Sustaining Work Program
  • Other: vocational rehabilitation
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
49 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Single blind, randomized control studySingle blind, randomized control study
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Effects of Vocational Rehabilitation Group Intervention on Motivation and Occupational Self-Awareness in Individuals With Intellectual Disabilities: A Single-Blind, Randomized Control Study
Actual Study Start Date :
Feb 6, 2020
Actual Primary Completion Date :
May 12, 2020
Actual Study Completion Date :
May 12, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention

The ENtering Employment and SUstaining Work (ENESUW) program consists of 6 main topics which are; "self-awareness", "occupational self-awareness", "taking responsibility", "teamwork and labor division", "problem identification" and "problem solving". The entire program adopts a very plain and easy to understand method of information transmission in order to facilitate lossless comprehension and strengthen the trust relationship between the therapists and the participants. The ENESUW program took 8 weeks in total with twice weekly sessions, making up a total of 16 structured group sessions. The group format enabled the participants to learn through meaningful peer interactions and group activities which were supportive of the main learning goals (i.e. group work, labor division and taking responsibility) of the program. The twice weekly sessions were 45 minutes long in order to keep the participants attentive and active throughout the program.

Other: The Entering Employment and Sustaining Work Program
A structured, motivation and self-awareness based group intervention
Other Names:
  • Occupational therapy - vocational rehabilitation
  • Other: vocational rehabilitation
    An individual based, focused on desired job or occupation, face-to-face intervention

    Active Comparator: control

    The control group also consisted of individuals with ID. They received face to face, individual vocational based occupational therapy approaches, which were twice a week for 8 weeks (approximately 40-45 minutes)

    Other: vocational rehabilitation
    An individual based, focused on desired job or occupation, face-to-face intervention

    Outcome Measures

    Primary Outcome Measures

    1. Occupational Self-Assessment version 2.2 (OSA 2.2) [Change from Baseline and to the 2 months]

      Occupational Self-Assessment (OSA) is a comprehensive assessment which was designed to collect information regarding the individuals' occupational self-awareness. The OSA is an entirely self-reported tool regarding occupational competence and value. The 21 item OSA evaluates skills (item 1-11), habituation (12-16) and volition (17-21). Each item contains two sets of 4-point Likert scales, the first scale is about the individuals' performance in various activities (1- I have a lot of problem doing this, 2 - I have some difficult doing this, 3 - I do this well, and 4 points = I do this extremely well) and the second scale is about the values of those activities for the individual 1 - This is not important to me, 2 - This is important to me, 3 -This is more important to me; and 4- This is most important to me)

    2. Objective Achievement Motivation Test - OLMT): [Change from Baseline and to the 2 months]

      The OLMT is a test which is used for Job & Career replacement and academic testing by assessing examinee's achievement motivation under different circumstances. The OLMT consists of 3 subtests, these 3 subtests include a particular stimulus that motivates respondent's performance: the task itself, setting own goals, and from competition. The test also evaluates the match or mismatch between the set goals and actual performance (aspiration level). For testing; the respondent requires to move a prescribed route cell by cell by pressing two buttons (red and green) repeatedly in ten seconds. For the aspiration level, the respondent sets a goal for the test and tries to accomplish the set goal by performing the first test. The final part the respondent competes against a virtual opponent whose speed is slightly above the mean of the first two tests of the respondent. The scoring of the test is performed by a special software

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 65 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    1. being between the ages of 18 and 65,

    2. Not being currently working,

    3. Having formal intellectual disability diagnosis,

    4. Having scored 23 points or less from the Mini Mental State Examination,

    5. Being able to understand basic Turkish language and 6) Volunteering to participate in the study

    Exclusion Criteria:
    1. Having severe communication problems specifically in self-expression,

    2. Not being able to continue participating in the study for the projected study duration,

    3. Not permitted to participate by legal guardian.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Hacettepe University Ankara Turkey

    Sponsors and Collaborators

    • Hacettepe University
    • Biruni University

    Investigators

    • Study Chair: Hülya Kayıhan, Prof, Occupational Therapy, head of department

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Orkun Tahir Aran, PhD., Hacettepe University
    ClinicalTrials.gov Identifier:
    NCT04728074
    Other Study ID Numbers:
    • 2020/34-18
    First Posted:
    Jan 28, 2021
    Last Update Posted:
    Jan 28, 2021
    Last Verified:
    Jan 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Orkun Tahir Aran, PhD., Hacettepe University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jan 28, 2021