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Clinical Trials/NCT06813001
NCT06813001Not yet recruitingNot Applicable

Development of ACT (Acceptance and Commitment Therapy)-Based Nurse-led Intervention for Ovarian Cancer Patients

Yonsei University0 sites25 target enrollmentStarted: February 1, 2025Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
25
Primary Endpoint
Change from baseline psychological distress on the last day of self-monitoring (Day 8)

Study Overview

Brief Summary

The purpose of this study is to evaluate the feasiblity and effectiveness of an Acceptance and Commitment Therapy (ACT)-based nursing intervention aimed at managing psychological flexibility, distress, anxiety, depression, fear of cancer recurrence/progression, quality of life, and symptoms. Patients will participate in a single online session with a nurse, followed by a daily self-monitoring survey online for one week. Data will be collected at baseline (prior to the ACT session), on day 8 (after one week of self-monitoring), and at 5 weeks. Primary outcome is psychological flexibility.

Detailed Description

This study is a preliminary single-group pre-post design aimed at developing and evaluating the feasibility of an ACT-based nursing intervention for distress management in patients with ovarian cancer. A total of 25 ovarian cancer patients who consent to participate will be enrolled in the study. Paticipants will receive a one-time ACT-based nursing intervention lasting approximately 60 minutes.

The researcher will coordinate schedules with participants to deliver the ACT-based nursing intervention using Zoom, a video conferencing platform which minimizes time and location constraints. Before the intervention, the research will ensure that the participants' video conferencing is working properly to minimize potential difficulties during the session.

Following the single-session intervention, the researcher will send a daily Google Form link to participants for seven consecutive days. Participants will be encouraged to access the link and complete self-monitoring surveys to reinforce the key components addressed in the program.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Single Group
Primary Purpose
Other
Masking
None

Eligibility Criteria

Ages
19 Years to 75 Years (Adult, Older Adult)
Sex
Female
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •adult (19 ≤ age ≤ 75).
  • •ovarian cancer patients with FIGO stage 2-
  • •Those who have completed first-line chemotherapy for ovarian cancer (excluding maintenance therapy) within the past 2 years.

Exclusion Criteria

  • •Patients with cognitive problems such as dementia or psychiatric problems such as major depression or generalized anxiety, or who are actively receiving treatment for any of these conditions.
  • •Patients with history of cancer recurrence.

Arms & Interventions

A

Experimental

Experimental group with application of ACT-based nursing intervention

Intervention: ACT-based nursing intervention (Other)

Outcomes

Primary Outcomes

Change from baseline psychological distress on the last day of self-monitoring (Day 8)

Time Frame: Psychological distress will be assessed at baseline and on the last day of self-monitoring (Day 8).

Psychological distress measured by Distress Thermometer.

Secondary Outcomes

  • Change from baseline depression(within 3 weeks after the last day of self-monitoring (window: 7 days))
  • Change from anxiety(within 3 weeks after the last day of self-monitoring (window: 7 days))
  • Change from fear of cancer recurrence(within 3 weeks after the last day of self-monitoring (window: 7 days))
  • Change from quality of life(within 3 weeks after the last day of self-monitoring (window: 7 days))
  • Change from psychological flexibility(within 3 weeks after the last day of self-monitoring (window: 7 days))
  • Change from symptoms(within 3 weeks after the last day of self-monitoring (window: 7 days))

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

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