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Family Counselling for Opioid Addiction

A Randomized Control Trial of Family Intervention for patients with Opioid Dependence

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/01/062107
Enrollment
100
Registered
2024-01-31
Start date
Unknown
Completion date
Unknown
Last updated
2024-03-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: F112- Opioid dependence

Interventions

Intervention1: Family Intervention: 3 sessions of family intervention each spaced 2 weeks apart Control Intervention1: Nil: Treatment as usual

Sponsors

AIIMS New Delhi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: For patients: Diagnosis of opioid dependence syndrome In early phase of maintenance treatment, either buprenorphine or naltrexone (initiated within 3 months) Willing to engage in the intervention Access to phone For family members: 1.Family member staying with the patient 2.Aged 18 and above 3.Planning to stay with the patient during the course of intervention and willing to participate in the family intervention 4.Patient willing to participate with the particular member in the intervention

Exclusion criteria

Exclusion criteria: For patients 1. Exposure to any structured psycho-social intervention for opioid use 2. Those who are intoxicated or in severe withdrawal which precludes an interview 3. Currently suffering from a psychotic illness 4. Psychiatric or medical comorbidity that precludes an interview For family members 1. Suffering from any substance use disorder except tobacco use disorder 2. Psychiatric or medical comorbidity that precludes an interview

Design outcomes

Primary

MeasureTime frame
To compare the change in family functioning of the family intervention group with the control group as measured on Family assessment device.Timepoint: At 0 and 12 weeks

Secondary

MeasureTime frame
To ascertain the therapist, patient and family member’s perspectives on family interventionTimepoint: after sessions;To compare the change of opioid use in the family intervention group with the control group.Timepoint: Baseline, 4 weeks, 8 weeks, 12 weeks

Countries

India

Contacts

Public ContactYesh Chandra Singh

Department of Psychiatry and NDDTC, AIIMS Delhi

sidsarkar22@gmail.com

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026