Validation of the Screen of Cancer Survivorship - Occupational Therapy Services (SOCS-OTS) Tool for Use in a Physical Medicine Rehabilitation Clinic

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Total Enrollment

80 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-07-12

Study Completion Date

2027-12-01

Brief Summary

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To compare the results of the SOCS-OTS to another standardized screening measure that is currently being used by rehabilitation services at MD Anderson Cancer Center and to ensure that the SOCS-OTS correctly identifies those individuals needing OT services in cancer care.

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Detailed Description

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Primary Aim

1\. Explore the SOCS-OTS for use in the Physical Medicine and Rehabilitation (PM\&R) clinic by means of diagnostic testing including sensitivity and specificity.

Secondary Aims

1. Explore whether the SOCS-OTS identifies the likelihood that the presence or absence of OT referral is correctly predicted. To accomplish this, the likelihood ratios, and predictive values of the SOCS-OTS will be assessed.
2. Determine associations between the need for OT and demographic factors such as stage of cancer, cancer treatment etc.
3. Establish test-retest reliability of the SOCS-OTS.

Conditions

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Cancer Occupational Therapy

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Screen of Cancer Survivorship - Occupational Therapy Services (SOCS-OTS)

You will be asked to complete three questionnaires and a short interview about yourself and how well you are able to complete your daily tasks. The SOCS-OTS, which is a 20-item questionnaire.

Screen of Cancer Survivorship - Occupational Therapy Services (SOCS-OTS)

Intervention Type OTHER

Given by Questionnaire

Interventions

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Screen of Cancer Survivorship - Occupational Therapy Services (SOCS-OTS)

Given by Questionnaire

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

1. Must be 18 years an older
2. Currently medically followed in the PMR clinic (with or without acute disease)
3. Must speak and read English. The AM-PAC is currently validated in adults only. Additionally, the assessment tools are in English without translation into other languages, therefore only clients who do speak and read English will be included. Pregnant participants are not excluded.

Exclusion Criteria

1\. Potential participants with confusion and cognitive impairments that might hinder their ability to sign an informed consent form or participate in the study.

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No