The Effect of Psychosocial Support on Improving Breast Cancer Patients Response to Medical Treatment

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age20-40
SponsorAl-Quds University

About this trial

The goal of this clinical trial is to evaluate the effect of psychosocial therapy on improving treatment response among breast cancer patients receiving chemotherapy. Participants will be randomized to receive standard medical treatment alone or combined with structured psychosocial therapy. Outcomes include treatment response, psychological well-being, and quality of life.

1. Do psychosocial interventions affect the response to breast cancer treatment? 2. How do societal attitudes toward psychological and social care influence the willingness of breast cancer patients in Palestine to seek psychosocial interventions?

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

age between 20-40 Being Palestinian female from west bank and Jerusalem

Diagnosed with stage I-III breast cancer.

Currently receiving active medical treatment.

Able to provide consent and participate in the intervention.

Disqualifiers

being male.

holding other nationalities than Palestinian or living outside the westbank or Jerusalem.

Younger than 20 or older than 40 years old.

Uncooperative with interviewer

Trial design

Design model

Parallel

Treatments tested in this trial

  • Psychosocial Therapy

    Behavioral

    The psychosocial therapy consists of structured, individual, in-person counseling sessions designed to provide emotional support, enhance coping skills, and address psychological and social challenges experienced by breast cancer patients during treatment. The intervention is delivered by trained mental health professionals and focuses on improving patients' psychological well-being and treatment response.

  • Standard Medical Treatment

    Other intervention

    Standard oncological medical treatment for breast cancer as prescribed by the treating physician, which may include chemotherapy, radiotherapy, hormonal therapy, or targeted therapy according to clinical guidelines.

Treatment groups

160 Participants
are divided into 2 treatment groups
Group A: Psychosocial interventionExperimental treatment 2 interventions
Group B: Standard medical treatmentActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Breast cancer-specific quality of life assessed by the Functional Assessment of Cancer Therapy - Breast (FACT-B)

Breast cancer-specific quality of life will be assessed using the Functional Assessment of Cancer Therapy-Breast (FACT-B) questionnaire. The FACT-B is a 37-item instrument assessing physical, social/family, emotional, functional well-being, and additional breast cancer concerns. Total scores range from 0 to 148, with higher scores indicating better quality of life.

Time frame
Baseline and 6 weeks

Secondary outcomes

1

Anxiety level assessed by the Hospital Anxiety and Depression Scale - Anxiety subscale (HADS-A)

Psychological distress will be assessed using the Hospital Anxiety and Depression Scale (HADS). The HADS is a 14-item questionnaire consisting of two subscales: anxiety and depression. Each subscale score ranges from 0 to 21, with higher scores indicating greater psychological distress and worse outcomes.

Time frame
Baseline and 6 weeks
2

Health-related quality of life assessed by the 36-item short form health survey (SF-36)

Health-related quality of life will be assessed using the Short Form-36 Health Survey (SF-36). The SF-36 is a 36-item questionnaire measuring eight domains of physical and mental health. Domain scores are transformed to a scale ranging from 0 to 100, with higher scores indicating better health-related quality of life.

Time frame
Baseline and 6 weeks

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: