Parents as the Primary Sexuality Educators for Their Young Adults With Down Syndrome

Sponsor
Advocate Health Care (Other)
Overall Status
Completed
CT.gov ID
NCT03135236
Collaborator
(none)
13
1
1
14.9
0.9

Study Details

Study Description

Brief Summary

By integrating sexuality and disability literatures, theories, and research methodologies, this study aims to: 1) contribute to the limited knowledge professionals have of parents as the primary sexuality educators; 2) create a resource for parents in order to be sexuality educators for their young adults with I/DD; and 3) evaluate the effectiveness of the Home B.A.S.E. for Developmental Disabilities Curriculum.

In order to meet the objectives the study seeks to answer the following questions:
  1. What is the effectiveness of a sexuality education workshop for parents of young adults with DS on improving the self-efficacy and attitudes around sexuality and healthy relationships for young adults with DS as well as increase the parent-child communication on sexuality topics?

  2. What are parents' concerns that impact their ability to be the primary sexuality educators for their young adults with DS? It is proposed that parent confidence and comfort talking about sexuality topics with their young adult with Down syndrome will increase thereby increasing the parent-child communication as a result of this study.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Parent training
N/A

Detailed Description

Enrollment will begin and will end once 30 eligible subjects have been identified. Anticipated duration is one year. Participants will enroll in one of the 4 different training series. Each series will have 3 dates they must attend. Once enrolled and consent is documented, eligible subject's will participate in the study for approximately three months. Participants will be expected to attend 3 training sessions over a 4 week period, each are up to 3 hours in length. There will be a follow-up post-survey one month after the last training and an optional phone interview that will occur 2 months after the final training. Participants will be compensated for their time with a $50 gift card once the final post-survey has been received. The gift card will be mailed to the family. Data analysis will begin once all trainings have been completed. Investigators anticipate completing the study, including primary analyses, within two years from the date recruitment begins.

Study Design

Study Type:
Interventional
Actual Enrollment :
13 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Parents as the Primary Sexuality Educators for Their Young Adults With Down Syndrome: The Effectiveness of a Family-based Training
Actual Study Start Date :
Mar 6, 2017
Actual Primary Completion Date :
Sep 30, 2017
Actual Study Completion Date :
Jun 1, 2018

Arms and Interventions

Arm Intervention/Treatment
Experimental: Parent training

All registered participants will participate in a series of trainings (3 separate) on sexuality education.

Behavioral: Parent training
Participants will attend 3 trainings. There will be a pre-test before training 1 and an initial post-test after training 3. There will be a final post-test 1 month after the final training.

Outcome Measures

Primary Outcome Measures

  1. Pre-survey, post-survey, and final post-survey [15-20 minutes]

    A paper survey will be completed before training 1 that gathers quantitative data that will address attitudes, self-efficacy, and behaviors of the parents in attendance. The survey will also be completed at the end of training 3 and then mailed to the participant to complete 1 month after the final training. The quantitative data will be used to measure a change in the attendees' attitudes, confidence, and behaviors before and after the proposed intervention. Data will be analyzed using SPSS.

Secondary Outcome Measures

  1. Qualitative data [5-15 minutes]

    Qualitative data will be collected at the end of the first and second training session with two to three take home open-ended questions for each participant to answer as well as after the training is over with open ended questions on the initial follow-up survey. Structured phone interviews will be completed with a small sample of the participants after the one month follow-up paper survey. Answers and interview questions will be transcribed, coded, and themes will be established.

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Parents of young adults with Down syndrome ages 20-30.

  • Be able to communicate in English

Exclusion Criteria:
  • Parents of young adults between the ages of 20 and 30 without Down syndrome

  • Parents of individuals with Down syndrome younger than 20 or older than 30.

  • Parents unable to attend 3 training sessions.

  • Not fluent English communicators.

  • Any vulnerable populations including pregnant women, neonates, prisoners, children, cognitively impaired adults, or adults unable to consent

Contacts and Locations

Locations

Site City State Country Postal Code
1 Advocate Adult Down Syndrome Center Park Ridge Illinois United States 60068

Sponsors and Collaborators

  • Advocate Health Care

Investigators

  • Principal Investigator: Katie Frank, PhD, OTR/L, Advocate Healthcare

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Katie Frank, PhD, OTR/L, Occupational therapist, Advocate Health Care
ClinicalTrials.gov Identifier:
NCT03135236
Other Study ID Numbers:
  • AdvocateHC
First Posted:
May 1, 2017
Last Update Posted:
Jun 18, 2018
Last Verified:
Jun 1, 2018
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 Katie Frank, PhD, OTR/L, Occupational therapist, Advocate Health Care
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 18, 2018