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CompletedNCT03571984MovingonABCUpdated Apr 12, 2023

Moving on After Breast Cancer Plus- for Breast Cancer Survivors

An interventional study of Moving on ABC Plus in Breast Cancer Female and Depression, sponsored by Pakistan Institute of Living and Learning. Completed at 1 site in Pakistan. Open to female participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2023-04-12.

Sponsored by Pakistan Institute of Living and Learning · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
354
Allocation
Randomized
Ages
18 Years and older
Sex
Female
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Study summary

Breast cancer (BC) ranks second among all the types of cancer and is equally common in developing as well as developed countries. Breast cancer is most common type of cancer worldwide and its diagnosis as well as early treatment is associated with distress. The aim of this study is to explore the feasibility of integrating a 'Moving on After Breast Cancer (ABC)' manual developed by service user (Dr A Saleem) with Cognitive Behavior Therapyfor Pakistani women who are breast cancer (BC) survivors attending primary care and oncology services in Pakistan B) refine the Moving on ABC plus so as to develop a culturally appropriate therapeutic programme to be tested in a future definitive randomized controlled trial.

Read the detailed description

According to an estimate of World Health Organization (2000) cancer was responsible for 12% of all the deaths from all causes worldwide and rate of cancer is expected to increase 50% by the year 2020. In Pakistan every ninth women has a chance of developing breast cancer, which is highest rate in Asia. The estimated incidence rate of breast cancer in Pakistan is 50/100,000. Despite the high association of distress with breast cancer, data on prevalence of depression in women with breast cancer especially in low income countries is limited .

The proposed project consists of two phases: 1) Phase 1: Integration of the two existing interventions Moving On ABC and the Cognitive Behavior Therapy and the refinement of the integrated intervention. 2) Phase 2: Randomized Control Trial (RCT). Sample size of Phase II will be comprised of 50 patients. Patients will be divided into two groups. One group will receive Group moving on ABC Plus intervention and other group will receive routine care. The total sample size of the effectiveness trial 354.

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Conditions studied

  • Breast Cancer Female
  • Depression

Keywords

  • Breast cancer
  • depression
  • Moving on ABC Plus
  • Pakistan
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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 enrollment of 354 is above the median of 72 across 9,303 interventional studies indexed under Breast Neoplasms.

Browse Breast Neoplasms studies →

Lead sponsor

Pakistan Institute of Living and Learning is the lead sponsor of 59 studies on the registry; 17 are open to participants now.

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

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
Female
Accepts healthy volunteers
No

Inclusion criteria

  • Female
  • Breast cancer (stage I to stage IV)
  • Has completed primary treatment for breast cancer
  • Score of 10 or above on PHQ - 9 or GAD - 7
  • Age 18 and above

Exclusion criteria

Exclusion Criteria:

  • Already diagnosed with any psychiatric illness
  • Already taking psychiatric medicines
  • Severe cognitive impairment (not able to give consent to take part in intervention)
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
354 participants (actual)

Study arms

  • Experimental
    Moving on ABC Plus

    Moving on ABC Plus is combination of two interventions. The culturally adapted CBT and Moving on ABC. CBT will be integrated with The Moving on After Breast Cancer (ABC), which has been developed by Dr Anneela Saleem who suffered from breast cancer. The integrated intervention will consist of 12 sessions (60-90 minutes). The first 8 sessions will be delivered weekly and the last four sessions will be delivered fortnightly

    Behavioral: Moving on ABC Plus

  • No intervention
    Routine Care

    This will consist of routine assessment and management as usually conducted by oncology clinics and general practice. GP's will be informed about the psychiatric diagnosis.

Interventions

  • BehavioralMoving on ABC Plus

    The intervention has two components. CBT Moving on After Breast Cancer

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What researchers measure

Primary outcomes

  1. Patient Health Questionnaire-9 (PHQ-9)

    Patient Health Questionnaire-9 (PHQ-9) will be used to diagnose depression.Minimum score of PHQ-9 is 0 and maximum score is 27. This scale categorizes depression in 5 different categories: minimal depression (score range 1-4), Mild depression (5-9), Moderate depression (10-14), Moderately severe depression (15-19), and Sever depression (20-27).

    Time frame: Changes from baseline to 4th and 6th month outcome

Secondary outcomes

  1. Generalized Anxiety Disorder - 7

    This is a short self-report measure to assess the presence and severity of generalized anxiety.

    Time frame: Changes from baseline to 4th and 6th month outcome

  2. EuroQol-5D (EQ-5D)

    EuroQol-5D (EQ-5D), a 5-itme scale, will be used to assess the quality of life. Lower raw score indicates better quality of life

    Time frame: Changes from baseline to 4th and 6th month outcome

  3. Multidimensional Scale for Perceived Social Support (MSPSS)

    Multidimensional Scale for Perceived Social Support (MSPSS) will be used to assess level of social support. Higher scores indicate higher level of support

    Time frame: Changes from baseline to 4th and 6th month outcome

  4. Intrusive Thoughts Scale

    We will measure Breast Cancer distress with the 7 item subscale of the revised Impact of Event Scale which is reported to be sensitive to change in BC survivors who are receiving a CBT intervention

    Time frame: Changes from baseline to 4th and 6th month outcome

  5. Rosenberg Self Esteem Scale

    This is a ten item Likert scale to measure self-esteem. Higher scores indicate better self esteem.

    Time frame: Changes from baseline to 4th and 6th month outcome

  6. The Functional Assessment of Cancer Therapy - Breast (FACT-B)

    This is one of the most widely used scales to measure health-related quality of life in BC patients. Minimum total score on the scale is "0" and maximum score is 148. Higher score on the scale indicate poor quality of life

    Time frame: Changes from baseline to 4th and 6th month outcome

  7. Client Satisfaction Questionnaire

    This is a well validated self-report measure of client/ patient satisfaction with health services. Minimum total score is "1" and maximum score is "32". Higher score indicate higher level of satisfaction with the services.

    Time frame: This will be administered at 4-month follow up

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Study locations

1 site
  • Civil Hospital
    Karachi, 75500, Pakistan
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References and documents

Publications

  • American cancer society (2010). The global economic cost of cancer. The American Cancer Society, Inc
  • Husain N, Chaudhry I, Raza-ur-Rehman, Ahmed GR. Self-esteem and obsessive compulsive disorder. J Pak Med Assoc. 2014 Jan;64(1):64-8. PubMed 24605716 ↗

Individual participant data

Plan to share: No

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 12, 2023, 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
NCT03571984
Lead sponsor
Pakistan Institute of Living and Learning
Responsible party
Sponsor
First posted
Jun 28, 2018
Start date
Mar 10, 2019
Primary completion
Dec 30, 2021
Completion
Jul 5, 2022
Last update
Apr 12, 2023

Study contacts

Nasim Chaudhry, MD
principal investigator · PILL

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Apr 2023. You cannot join it, but the record below documents what was studied.

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