Skip to main content
OpenTrials
Recruiting

NCT Number: NCT06329531

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

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.

Recruiting

Interested in participating?

Request Info

Key information

Conditions

Cancer Neoplasms Occupational Therapy

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

MD Anderson Cancer Center

Houston, Texas, 77030, United States

Location status: Recruiting

Location contact

Ekta Gupta, MD

CONTACT

[email protected]

713-745-2327

Ekta Gupta, MD

PRINCIPAL_INVESTIGATOR

About this study

Primary Aim

  • 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

  • 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.
  • Determine associations between the need for OT and demographic factors such as stage of cancer, cancer treatment etc.
  • Establish test-retest reliability of the SOCS-OTS.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Must be 18 years an older
  • Currently medically followed in the PMR clinic (with or without acute disease)
  • 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

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

Treatment and study plan

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

Other

Given by Questionnaire

Primary outcomes

  1. Safety and adverse events (AEs)

    Time frame: Through study completion; an average of 1 year.

    Incidence of Adverse Events, Graded According to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE)

Study contacts

Contact information is provided by the study sponsor or research team.

Ekta Gupta, MD

CONTACT

[email protected]

(713) 745-2327

Sponsors and collaborators

Lead sponsor

M.D. Anderson Cancer Center

Other

Registry information

Important dates

Study start
2024
Primary completion
2027
Study completion
2027
First posted
Mar 26, 2024
Registry last updated
Apr 16, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Related clinical trials

Published trials that share one or more normalized conditions with this study.