CClinicalTrials.gg
Status unknownNCT00279474Updated Jan 19, 2006

The Effect of Cognitive Behavior Intervention on Psychological Distress of Cancer Patients and Their Family Members

An interventional study of cognitive-behavior groups in Cancer, sponsored by Rambam Health Care Campus. Status unknown at 1 site in Israel. Open to participants aged 20 Years to 70 Years. Per ClinicalTrials.gov, last updated 2006-01-19.

Sponsored by Rambam Health Care Campus · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Oct 2005), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
320
Allocation
Randomized
Ages
20 Years to 70 Years
Sex
All
01

Study summary

The aim of the study is to evaluate the effect of cognitive behavior group intervention with cancer patients and their family members. Around 80 cancer patients and their family members will participate in group intervention and will be compared with 80 controls.

Read the detailed description

The aim of the study is to evaluate the effect of cognitive behavior group intervention with cancer patients and their family members. Around 80 cancer patients and their family members will participate in group intervention and will be compared with 80 controls (randomized control study). Brief Symptom Inventory,Fatigue inventory, Mini Sleep Questionnaire and repression-sensitization questionnaire will be answered by the participants pre-, post-intervention and after four months.

02

Conditions studied

  • Cancer

Keywords

  • cancer patients
  • family
  • cognitive behavior
  • distress
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In context

Lead sponsor

Rambam Health Care Campus is the lead sponsor of 456 studies on the registry; 33 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

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

Inclusion criteria

  • Hebrew speaking

Exclusion criteria

Exclusion Criteria:

  • psychiatric condition
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
320 participants

Interventions

  • Behavioralcognitive-behavior groups
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What researchers measure

Primary outcomes

  1. Reduction in psychological distress, level of fatigue and sleep problems

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Study locations

1 of 1 sites recruiting
  • Rambam medical center, Oncology department
    Haifa, Israel
    Recruiting
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 19, 2006, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT00279474
Lead sponsor
Rambam Health Care Campus
First posted
Jan 19, 2006
Start date
Jul 2004
Completion
Dec 2005
Last update
Jan 19, 2006

Study contacts

Miri Cohen
Contact
cohenm@research.haifa.ac.il
972 523 688623
Georgeta Fried
Contact
972 4 853018
Miri Cohen, PhD
principal investigator · Rambam Health Care Campus
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Oct 2005. You cannot join it, but the record below documents what was studied.

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