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RecruitingNCT06808828IPVUpdated Aug 4, 2026

Occupational Therapy for Adults Who Have Experienced Intimate Partner Violence (IPV)

An interventional study of Health and coping skills in Domestic Violence, sponsored by Loma Linda University. Recruiting at 1 site in United States. Open to participants aged 18 Years to 70 Years. Per ClinicalTrials.gov, last updated 2026-08-04.

Sponsored by Loma Linda University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
25
Allocation
Not applicable
Ages
18 Years to 70 Years
Sex
All
01

Study summary

The purpose of this graduate student research study is to understand the effectiveness of an occupational therapy program in a domestic violence shelter. It is expected that participation will last about 6 weeks. Subjects will complete pretests involving lifestyle assessments and a coping scale and then participate in 8 occupational therapy sessions during the 4 weeks of program implementation. The occupational therapy sessions will last approximately 90 minutes. After the program is completed, subjects will complete the posttests.

Procedures and Activities. You will be asked to:

Complete a series of questionnaires about your health, well-being, and daily activities.

Participate in 8 OT sessions that may include activities such as journaling, positive self-talk, coping skills methods, and grounding exercises.

Complete the posttests.

02

Conditions studied

  • Domestic Violence

Keywords

  • domestic violence
  • intimate partner violence
  • occupational therapy
03

Who can participate

Ages eligible
18 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Male or Female 18 years of age or older receiving services from a domestic violence organization

Exclusion criteria

Exclusion Criteria:

  • None
04

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
25 participants (estimated)

Study arms

  • Experimental
    Health and coping skills

    Subjects will complete an 8-item occupational therapy lifestyle medicine checklist at each session. The subjects will participate in eight sessions receiving education on health topics of sleep hygiene, physical activity, healthy cooking, self-management, coping skills, self-esteem, mindfulness, and goal setting.

    Behavioral: Health and coping skills

Interventions

  • BehavioralHealth and coping skills

    An occupational therapist and occupational therapy graduate capstone student will lead in-person sessions. Subjects will participate in an occupational therapy program that meets 2x/week x 4 weeks for eight sessions. Topics will include sleep hygiene, physical activity, healthy cooking, self-management, coping skills, self-esteem, mindfulness, and goal setting. Subjects will receive education as well as actively engage in activities related to the topic. Subjects will be provided with a personal journal to complete homework involving reflections on the topics discussed in the sessions.

05

What researchers measure

Primary outcomes

  1. Improvement in Healthy Lifestyle

    This is a composite measurement, utilizing the Occupational Therapy Lifestyle Medicine Checklist (OTLM) to assess improvement in the following categories: Healthy eating; Physical Activity; Stress Management; Social Connections; Sleep; Work/School (that's too vague to measure), Leisure and Hobbies; Avoiding Risky Substances. Participants will complete this checklist at baseline, prior to the first intervention and after the final eight intervention is completed. Each category will have a range (1-10), which will indicate how the participant has responded overall to the intervention. An overall increase of \>15 points in the combined categories will indicate significant improvement. An overall decrease of any number of points will indicate non-significant improvement.

    Time frame: Change between baseline assessment at initial enrollment and completion of Session 8 at 8 weeks post-enrollment.

  2. Improvement in Quality of Life

    This is a compositive measure utilizing the 36-Item Short Form Health Survey Questionnaire. Quality of life involves several areas. The 36-item Short Form is a self-reported measure that consists of thirty-six questions covering eight domains of health. Categories include (1) limitations in physical activities, (2) limitations in social activities, (3) limitations in usual role activities because of physical health problems, (4) bodily pain, (5) general mental health, (6) limitations in usual role activities because of emotional problems, (7) vitality, and (8) general health perceptions. Subjects may receive a score ranging from 0-100. Higher scores indicate more favorable health.

    Time frame: Change between the baseline assessment and post-test at study completion, up to 9 weeks post-enrollment

  3. Improvement in Coping Skills

    This is a composite measure that will utilize the Coping Scale Questionnaire. This 13-item questionnaire gathers information on how the subject copes. Categories include anger management, endurance, well-being, and posttraumatic growth. Higher scores indicate higher levels of coping.

    Time frame: Change between the baseline assessment and post-test at study completion, up to 9 weeks post-enrollment.

06

Study locations

1 of 1 sites recruiting
  • Loma Linda University Health
    Loma Linda, California 92350, United States
    Recruiting
07

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT06808828
Lead sponsor
Loma Linda University
Responsible party
Sponsor
First posted
Feb 5, 2025
Start date
Feb 3, 2025
Primary completion
Dec 2026 (estimated)
Completion
Dec 2026 (estimated)
Last update
Aug 4, 2026

Study contacts

Heather Javaherian, OTD
Contact
hjavaherian@llu.edu
9095584628
Leticia Guerrero, BA
Contact
letguerrero@llu.edu
909-558-4628
Heather Javaherian, OTD
principal investigator · Loma Linda University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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