CClinicalTrials.gg
Status unknownNCT02934815BC-SEGTUpdated Oct 17, 2016

Relational and Emotional Mechanisms of a Supportive-expressive Group Intervention in Breast Cancer

An interventional study of Supportive-expressive group therapy in Breast Neoplasms and Breast Cancer, sponsored by Universidade do Porto. Status unknown at 1 site in Portugal. Open to female participants aged 30 Years to 65 Years. Per ClinicalTrials.gov, last updated 2016-10-17.

Sponsored by Universidade do Porto · Not applicable, Interventional, and Supportive care

The sponsor has not verified this record recently (last verified Oct 2016), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
50
Allocation
Non-randomized
Ages
30 Years to 65 Years
Sex
Female
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Study summary

To test the feasibility of supportive-expressive group intervention (SEGT) for women with primary breast cancer and to provide a preliminary test of its efficacy.

Read the detailed description

This study aims to compare the efficacy of a 16-sessions group intervention (Supportive-Expressive group therapy) versus control group (no intervention) in women with primary breast cancer.

This study tries to evaluate the efficacy of SEGT on breast cancer patients' emotion regulation, social support, caregiving, and marital satisfaction, and its improvement on breast cancer patients' life quality. This study also intents to explore the moderating role of attachment on these associations.

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Conditions studied

  • Breast Neoplasms
  • Breast Cancer

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Keywords

  • psychological intervention
  • breast cancer
  • supportive-expressive group therapy
  • emotion regulation
  • social support
  • attachment
  • quality of life
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In context

Breast Neoplasms

12,544 studies on the registry are indexed under Breast Neoplasms; 2,892 are open to participants now.

This study's planned enrollment of 50 is below the median of 72 across 9,303 interventional studies indexed under Breast Neoplasms.

Browse Breast Neoplasms studies →

Lead sponsor

Universidade do Porto is the lead sponsor of 170 studies on the registry; 52 are open to participants now.

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

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Who can participate

Ages eligible
30 Years to 65 Years
Sexes eligible
Female
Accepts healthy volunteers
No

Inclusion criteria

  • diagnosis of primary breast cancer

Exclusion criteria

Exclusion Criteria:

  • attendance at a cancer support group or individual psychotherapy
  • diagnosis of recurrent breast cancer
  • severe psychiatric disorder
  • history of drug or alcohol abuse
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Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
50 participants (estimated)

Study arms

  • Experimental
    Intervention group - SEGT

    16 weekly sessions, 90 min of Supportive-expressive group therapy

    Other: Supportive-expressive group therapy

  • No intervention
    Control group

    No intervention

Interventions

  • OtherSupportive-expressive group therapy

    The supportive-expressive group therapy (SEGT) is an intervention for women with BC that is designed to build bonds and to facilitate changes in emotional expression and regulation taking into account the role that emotions play in physiologic function, intimately related to the progression of the disease. It is based on seven main themes: building bonds, expressing feelings, detoxifying dying, reordering life priorities, improve support from and communication with family and friends, fortifying families, dealing with doctors, and control pain and anxiety. Although originally developed according to an existential perspective, recently the supportive-expressive group therapy has been used according to an attachment framework.

    Also known as: SEGT

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What researchers measure

Primary outcomes

  1. Change in quality of life across time

    The World Health Organization Quality of Life - BREF

    Time frame: T0 - before the intervention; T1 - 2 months later; T2 - 4 months later; T3 - 10 months later

Secondary outcomes

  1. Change in emotion suppression across time

    The Emotion Regulation Questionnaire

    Time frame: T0 - before the intervention; T1 - 2 months later; T2 - 4 months later; T3 - 10 months later

  2. Change in emotional self-efficacy across time

    The Stanford Emotional Self-Efficacy Scale-Cancer

    Time frame: T0 - before the intervention; T1 - 2 months later; T2 - 4 months later; T3 - 10 months later

  3. Change in cognitive emotion across time

    The Cognitive Emotion Regulation Questionnaire

    Time frame: T0 - before the intervention; T1 - 2 months later; T2 - 4 months later; T3 - 10 months later

  4. Change in social support across time

    The Multidimensional Scale of Perceived Social Support

    Time frame: T0 - before the intervention; T1 - 2 months later; T2 - 4 months later; T3 - 10 months later

  5. Change in caregiving across time

    The Caregiving Questionnaire

    Time frame: T0 - before the intervention; T1 - 2 months later; T2 - 4 months later; T3 - 10 months later

  6. Change in marital relationship across time

    Relationship Assessment Scale

    Time frame: T0 - before the intervention; T1 - 2 months later; T2 - 4 months later; T3 - 10 months later

Other outcomes

  1. Change in group climate across time

    The Group Climate Questionnaire

    Time frame: T1 - 2 months later; T2 - 4 months later; T3 - 10 months later

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Study locations

1 of 1 sites recruiting
  • Tânia Brandão
    Porto, 4200-135, Portugal
    Recruiting
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 17, 2016, 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
NCT02934815
Lead sponsor
Universidade do Porto
Collaborators
Fundação para a Ciência e a Tecnologia, Centro Hospitalar de Vila Nova de Gaia/Espinho, Centro Hospitalar De São João, E.P.E., Mama Help - Support Centre for Breast Cancer Patients
Responsible party
Tânia Brandão (Ph.D. Student, Universidade do Porto) — Principal investigator
First posted
Oct 17, 2016
Start date
Jan 2015
Primary completion
Jan 2017 (estimated)
Completion
Jan 2017 (estimated)
Last update
Oct 17, 2016

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Oct 2016. You cannot join it, but the record below documents what was studied.

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