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Effect of MSD on FCR Among Gastric Cancer Survivors

U

University of Malaya

Status

Enrolling

Conditions

Stomach Cancer;Clinical Control Trial

Treatments

Behavioral: Marital self disclosure

Study type

Interventional

Funder types

Other

Identifiers

NCT05606549
18801155781

Details and patient eligibility

About

The goal of this clinical trial is to explores the effect of marital self disclosure intervention on fear of cancer recurrence and dyadic coping ability in gastric cancer survivors and their spouses. The main questions are: What is the level of fear of cancer recurrence among gastric cancer survivors and their spouse? What is the level of dyadic coping ability among gastric cancer survivors and their spouse?What is the effect of marital self-disclosure intervention on fear of cancer recurrence and dyadic coping ability in the gastric cancer survivors and their spouses? Participants will accept the intervention of marital self disclosure for 4 times (4 cycles of chemotherapy) with different topics. Researchers will compare with control group to see if the level of fear of cancer recurrence and dyadic coping ability will be improved.

Enrollment

84 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • The disease meets the diagnostic criteria of "Guidelines for Diagnosis and Treatment of Gastric Cancer"(Department of Medical Affairs, 2019), the preoperative gastroscopy and pathological diagnosis are advanced gastric cancer, and the postoperative pathological classification is type II, III or IV
  • Age ≥ 18 years
  • Able to write and oral communicate effectively by themself
  • The main caregiver is their spouse
  • Clear consciousness, no understanding barriers
  • Agree to participate in this study

Exclusion criteria

  • History of receiving a structured psychological intervention from a psychiatrist or a psychologist
  • Cognitive disorders or psychiatric disorders (according to the DSM-V)
  • Severe visual, hearing and speech impairment
  • With previous or concurrent malignant tumors
  • With severe complications, such as gastrointestinal obstruction, perforation, etc.

Trial design

Primary purpose

Supportive Care

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

84 participants in 2 patient groups

marital self disclosure
Experimental group
Treatment:
Behavioral: Marital self disclosure
Routine care
No Intervention group

Trial contacts and locations

1

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Central trial contact

Zhou Ye

Data sourced from clinicaltrials.gov

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